BR112020011746A2 - compostos heterocíclicos bicíclicos substituídos atuando como inibidores de prmt5 - Google Patents

compostos heterocíclicos bicíclicos substituídos atuando como inibidores de prmt5 Download PDF

Info

Publication number: BR112020011746A2
Authority: BR; Brazil
Prior art keywords: amino; pyrimidine; pyrrolo; compound; diol
Prior art date: 2017-12-13

Application number

BR112020011746-3A

Other languages

English (en)

Portuguese (pt)

Inventor

Prathap Sreedharan Nair

Sanjeev Anant KULKARNI

Milind Dattatraya Sindkhedkar

Venkata P. Palle

Rajender Kumar Kamboj

Ganesh Bhausaheb GUDADE

Sachin Sethi

Dipak Raychand Lagad

Chetan Sanjay Pawar

Mahadeo Bhaskar Tryambake

Chaitanya Prabhakar KULKARNI

Anil Kashiram Hajare

Balasaheb Arjun Gore

Original Assignee

Lupin Limited

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2017-12-13

Filing date

2018-12-13

Publication date

2020-11-17

2018-12-13 Application filed by Lupin Limited filed Critical Lupin Limited

2020-11-17 Publication of BR112020011746A2 publication Critical patent/BR112020011746A2/pt

Links

125000002618 bicyclic heterocycle group Chemical group 0.000 title abstract description 3
239000003112 inhibitor Substances 0.000 title description 5
101150097768 prmt5 gene Proteins 0.000 title 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 67
238000011282 treatment Methods 0.000 claims abstract description 51
150000003839 salts Chemical class 0.000 claims abstract description 43
208000035475 disorder Diseases 0.000 claims abstract description 34
201000010099 disease Diseases 0.000 claims abstract description 33
238000000034 method Methods 0.000 claims abstract description 30
239000008194 pharmaceutical composition Substances 0.000 claims abstract description 16
102100034607 Protein arginine N-methyltransferase 5 Human genes 0.000 claims abstract 8
101710084427 Protein arginine N-methyltransferase 5 Proteins 0.000 claims abstract 8
150000001875 compounds Chemical class 0.000 claims description 627
-1 -NH> 2 Substances 0.000 claims description 479
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 196
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 94
VQWAZBMRMSMLPG-UHFFFAOYSA-N cyclopent-3-ene-1,2-diol Chemical compound OC1CC=CC1O VQWAZBMRMSMLPG-UHFFFAOYSA-N 0.000 claims description 89
238000002360 preparation method Methods 0.000 claims description 76
125000000217 alkyl group Chemical group 0.000 claims description 56
JLAWMIBCQHKGAN-UHFFFAOYSA-N bicyclo[3.1.0]hexane-2,3-diol Chemical compound OC1C(O)CC2CC21 JLAWMIBCQHKGAN-UHFFFAOYSA-N 0.000 claims description 47
229910052739 hydrogen Inorganic materials 0.000 claims description 40
239000001257 hydrogen Substances 0.000 claims description 39
125000000753 cycloalkyl group Chemical group 0.000 claims description 35
206010028980 Neoplasm Diseases 0.000 claims description 30
210000004027 cell Anatomy 0.000 claims description 29
125000000623 heterocyclic group Chemical group 0.000 claims description 24
150000002431 hydrogen Chemical class 0.000 claims description 22
229910052801 chlorine Inorganic materials 0.000 claims description 20
229910052736 halogen Inorganic materials 0.000 claims description 20
125000001072 heteroaryl group Chemical group 0.000 claims description 19
230000005764 inhibitory process Effects 0.000 claims description 19
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 18
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 15
150000002367 halogens Chemical class 0.000 claims description 15
229910052760 oxygen Inorganic materials 0.000 claims description 13
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
125000003118 aryl group Chemical group 0.000 claims description 12
208000011580 syndromic disease Diseases 0.000 claims description 11
201000011510 cancer Diseases 0.000 claims description 10
229910052794 bromium Inorganic materials 0.000 claims description 9
229910052799 carbon Inorganic materials 0.000 claims description 9
125000004093 cyano group Chemical group *C#N 0.000 claims description 9
229910052731 fluorine Inorganic materials 0.000 claims description 9
125000001188 haloalkyl group Chemical group 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 8
229910052717 sulfur Inorganic materials 0.000 claims description 8
208000025205 Mantle-Cell Lymphoma Diseases 0.000 claims description 7
208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims description 7
208000024893 Acute lymphoblastic leukemia Diseases 0.000 claims description 6
208000014697 Acute lymphocytic leukaemia Diseases 0.000 claims description 6
208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 claims description 6
206010005003 Bladder cancer Diseases 0.000 claims description 6
206010006187 Breast cancer Diseases 0.000 claims description 6
208000026310 Breast neoplasm Diseases 0.000 claims description 6
206010008342 Cervix carcinoma Diseases 0.000 claims description 6
208000010833 Chronic myeloid leukaemia Diseases 0.000 claims description 6
206010009944 Colon cancer Diseases 0.000 claims description 6
208000001333 Colorectal Neoplasms Diseases 0.000 claims description 6
201000010915 Glioblastoma multiforme Diseases 0.000 claims description 6
208000034578 Multiple myelomas Diseases 0.000 claims description 6
208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 claims description 6
208000002454 Nasopharyngeal Carcinoma Diseases 0.000 claims description 6
206010061306 Nasopharyngeal cancer Diseases 0.000 claims description 6
206010029260 Neuroblastoma Diseases 0.000 claims description 6
206010033128 Ovarian cancer Diseases 0.000 claims description 6
206010061535 Ovarian neoplasm Diseases 0.000 claims description 6
206010061902 Pancreatic neoplasm Diseases 0.000 claims description 6
206010035226 Plasma cell myeloma Diseases 0.000 claims description 6
208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims description 6
206010060862 Prostate cancer Diseases 0.000 claims description 6
208000000236 Prostatic Neoplasms Diseases 0.000 claims description 6
206010039491 Sarcoma Diseases 0.000 claims description 6
206010041067 Small cell lung cancer Diseases 0.000 claims description 6
208000003721 Triple Negative Breast Neoplasms Diseases 0.000 claims description 6
208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 6
208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims description 6
201000010881 cervical cancer Diseases 0.000 claims description 6
208000005017 glioblastoma Diseases 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 6
201000001441 melanoma Diseases 0.000 claims description 6
201000011216 nasopharynx carcinoma Diseases 0.000 claims description 6
125000004043 oxo group Chemical group O=* 0.000 claims description 6
201000002528 pancreatic cancer Diseases 0.000 claims description 6
208000008443 pancreatic carcinoma Diseases 0.000 claims description 6
208000000587 small cell lung carcinoma Diseases 0.000 claims description 6
208000022679 triple-negative breast carcinoma Diseases 0.000 claims description 6
201000005112 urinary bladder cancer Diseases 0.000 claims description 6
208000031261 Acute myeloid leukaemia Diseases 0.000 claims description 5
VUJZADUMJKDXEG-NJYVYQBISA-N CC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound CC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O VUJZADUMJKDXEG-NJYVYQBISA-N 0.000 claims description 5
BMXJTBWMARBKQI-SELNLUPBSA-N C[C@]1(O)[C@@H](O)[C@@H](C=C1CCC1=CC(F)=C2C=C(Cl)C(N)=NC2=C1)N1C=CC2=C1N=CN=C2N Chemical compound C[C@]1(O)[C@@H](O)[C@@H](C=C1CCC1=CC(F)=C2C=C(Cl)C(N)=NC2=C1)N1C=CC2=C1N=CN=C2N BMXJTBWMARBKQI-SELNLUPBSA-N 0.000 claims description 5
206010014733 Endometrial cancer Diseases 0.000 claims description 5
206010014759 Endometrial neoplasm Diseases 0.000 claims description 5
208000031671 Large B-Cell Diffuse Lymphoma Diseases 0.000 claims description 5
208000033776 Myeloid Acute Leukemia Diseases 0.000 claims description 5
GDCLGNZMJYZLOW-NJYVYQBISA-N NC1=NC2=CC(=CC(=C2C=C1Br)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC2=C1N=CN=C2C)O)O Chemical compound NC1=NC2=CC(=CC(=C2C=C1Br)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC2=C1N=CN=C2C)O)O GDCLGNZMJYZLOW-NJYVYQBISA-N 0.000 claims description 5
LIGWWSBYNROVSQ-QRVBRYPASA-N NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=C(F)C=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=C(F)C=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O LIGWWSBYNROVSQ-QRVBRYPASA-N 0.000 claims description 5
BGYHROJFKZIRTE-QRVBRYPASA-N NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Br)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Br)C(N)=NC3=C2)[C@@H](O)[C@H]1O BGYHROJFKZIRTE-QRVBRYPASA-N 0.000 claims description 5
PARWBKYZOJNTEO-QRVBRYPASA-N NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O PARWBKYZOJNTEO-QRVBRYPASA-N 0.000 claims description 5
208000005718 Stomach Neoplasms Diseases 0.000 claims description 5
125000003545 alkoxy group Chemical group 0.000 claims description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
206010012818 diffuse large B-cell lymphoma Diseases 0.000 claims description 5
201000003914 endometrial carcinoma Diseases 0.000 claims description 5
206010017758 gastric cancer Diseases 0.000 claims description 5
206010073071 hepatocellular carcinoma Diseases 0.000 claims description 5
208000014018 liver neoplasm Diseases 0.000 claims description 5
208000002154 non-small cell lung carcinoma Diseases 0.000 claims description 5
201000011549 stomach cancer Diseases 0.000 claims description 5
208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims description 5
208000035518 Squamous cell carcinoma of the oropharynx Diseases 0.000 claims description 4
239000003814 drug Substances 0.000 claims description 4
125000005842 heteroatom Chemical group 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
206010041823 squamous cell carcinoma Diseases 0.000 claims description 4
XTKQUHMFRARNRF-AMJAIQEXSA-N (1S,2R,5R)-3-[1-(2-amino-3-bromoquinolin-7-yl)propan-2-yl]-5-(4-aminopyrrolo[2,3-d]pyrimidin-7-yl)cyclopent-3-ene-1,2-diol Chemical compound CC(CC1=CC=C2C=C(Br)C(N)=NC2=C1)C1=C[C@H]([C@H](O)[C@@H]1O)N1C=CC2=C1N=CN=C2N XTKQUHMFRARNRF-AMJAIQEXSA-N 0.000 claims description 3
VIDCJEBGJMFJFH-AMJAIQEXSA-N CC(CC1=CC=C2C=C(Cl)C(N)=NC2=C1)C1=C[C@H]([C@H](O)[C@@H]1O)N1C=CC2=C1N=CN=C2N Chemical compound CC(CC1=CC=C2C=C(Cl)C(N)=NC2=C1)C1=C[C@H]([C@H](O)[C@@H]1O)N1C=CC2=C1N=CN=C2N VIDCJEBGJMFJFH-AMJAIQEXSA-N 0.000 claims description 3
RUJPBLSHGVJXKO-VSKRKVRLSA-N CCC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound CCC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(F)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O RUJPBLSHGVJXKO-VSKRKVRLSA-N 0.000 claims description 3
GSWCAJLANVNHPV-JXALWOEJSA-N CC[C@]1(O)[C@@H](O)[C@@H](C=C1CCC1=CC(F)=C2C=C(Cl)C(N)=NC2=C1)N1C=CC2=C1N=CN=C2N Chemical compound CC[C@]1(O)[C@@H](O)[C@@H](C=C1CCC1=CC(F)=C2C=C(Cl)C(N)=NC2=C1)N1C=CC2=C1N=CN=C2N GSWCAJLANVNHPV-JXALWOEJSA-N 0.000 claims description 3
NDQDXHNULILYQO-MZYLBHOOSA-N NC1=NC2=CC(=CC(=C2C=C1Cl)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC2=C1N=CN=C2C(C)C)O)O Chemical compound NC1=NC2=CC(=CC(=C2C=C1Cl)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC2=C1N=CN=C2C(C)C)O)O NDQDXHNULILYQO-MZYLBHOOSA-N 0.000 claims description 3
BYYNFTIVTRZVBL-QRVBRYPASA-N NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(Cl)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC(Cl)=C3C=C(Cl)C(N)=NC3=C2)[C@@H](O)[C@H]1O BYYNFTIVTRZVBL-QRVBRYPASA-N 0.000 claims description 3
KGEDWSNKYWOIDW-LZQZEXGQSA-N NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC=C3C=C(Cl)C(N)=NC3=C2F)[C@@H](O)[C@H]1O Chemical compound NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC=C3C=C(Cl)C(N)=NC3=C2F)[C@@H](O)[C@H]1O KGEDWSNKYWOIDW-LZQZEXGQSA-N 0.000 claims description 3
201000009030 Carcinoma Diseases 0.000 claims description 2
UGZKLGXHJGPADD-JRFVFWCSSA-N NC1=NC2=CC(=CC(=C2C=C1Cl)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC2=C1N=CN=C2C=1C=NN(C=1)C)O)O Chemical compound NC1=NC2=CC(=CC(=C2C=C1Cl)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC2=C1N=CN=C2C=1C=NN(C=1)C)O)O UGZKLGXHJGPADD-JRFVFWCSSA-N 0.000 claims description 2
XDALKOHBSHKPME-QRVBRYPASA-N NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC=C3C=C(Br)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC=C3C=C(Br)C(N)=NC3=C2)[C@@H](O)[C@H]1O XDALKOHBSHKPME-QRVBRYPASA-N 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
239000003937 drug carrier Substances 0.000 claims description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
239000002131 composite material Substances 0.000 claims 5
CVEFDUOXWWDNET-UHFFFAOYSA-N 3-bromoquinolin-2-amine Chemical compound C1=CC=C2C=C(Br)C(N)=NC2=C1 CVEFDUOXWWDNET-UHFFFAOYSA-N 0.000 claims 1
BWAKDSWHFFKXKL-ZLNRFVROSA-N NC1=NC2=CC(=CC(=C2C=C1Cl)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC=2C(=NC=CC=21)C)O)O Chemical compound NC1=NC2=CC(=CC(=C2C=C1Cl)F)CCC=1[C@H]([C@H]([C@@H](C=1)N1C=CC=2C(=NC=CC=21)C)O)O BWAKDSWHFFKXKL-ZLNRFVROSA-N 0.000 claims 1
PEDIVUVDUFEXNM-UHFFFAOYSA-N NC1=NC=NC2=C1C=CN2C1C=CC(O)C1(O)CCC1=CC=C2C=C(F)C(N)=NC2=C1 Chemical compound NC1=NC=NC2=C1C=CN2C1C=CC(O)C1(O)CCC1=CC=C2C=C(F)C(N)=NC2=C1 PEDIVUVDUFEXNM-UHFFFAOYSA-N 0.000 claims 1
230000002496 gastric effect Effects 0.000 claims 1
230000002018 overexpression Effects 0.000 abstract description 10
238000004895 liquid chromatography mass spectrometry Methods 0.000 description 438
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 329
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 315
238000005481 NMR spectroscopy Methods 0.000 description 263
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 131
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 123
238000006243 chemical reaction Methods 0.000 description 121
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 120
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 106
235000019439 ethyl acetate Nutrition 0.000 description 105
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 98
239000012044 organic layer Substances 0.000 description 96
238000005160 1H NMR spectroscopy Methods 0.000 description 95
239000011541 reaction mixture Substances 0.000 description 95
239000000203 mixture Substances 0.000 description 80
238000010828 elution Methods 0.000 description 77
239000000243 solution Substances 0.000 description 75
239000007787 solid Substances 0.000 description 74
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 63
239000003208 petroleum Substances 0.000 description 61
239000007858 starting material Substances 0.000 description 58
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 54
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 50
239000012267 brine Substances 0.000 description 49
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 49
239000000543 intermediate Substances 0.000 description 48
239000000460 chlorine Substances 0.000 description 46
239000010410 layer Substances 0.000 description 40
KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 33
DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 33
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 32
238000003756 stirring Methods 0.000 description 32
SQVRNKJHWKZAKO-PFQGKNLYSA-N N-acetyl-beta-neuraminic acid Chemical compound CC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-PFQGKNLYSA-N 0.000 description 28
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 28
150000001412 amines Chemical class 0.000 description 27
229920006395 saturated elastomer Polymers 0.000 description 27
CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 26
241000065675 Cyclops Species 0.000 description 26
GCMNJUJAKQGROZ-UHFFFAOYSA-N 1,2-Dihydroquinolin-2-imine Chemical compound C1=CC=CC2=NC(N)=CC=C21 GCMNJUJAKQGROZ-UHFFFAOYSA-N 0.000 description 25
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 24
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 23
LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 23
239000012071 phase Substances 0.000 description 23
239000011734 sodium Substances 0.000 description 22
ABADUMLIAZCWJD-UHFFFAOYSA-N 1,3-dioxole Chemical compound C1OC=CO1 ABADUMLIAZCWJD-UHFFFAOYSA-N 0.000 description 21
JJTNLWSCFYERCK-UHFFFAOYSA-N 7h-pyrrolo[2,3-d]pyrimidine Chemical compound N1=CN=C2NC=CC2=C1 JJTNLWSCFYERCK-UHFFFAOYSA-N 0.000 description 21
AMKGKYQBASDDJB-UHFFFAOYSA-N 9$l^{2}-borabicyclo[3.3.1]nonane Chemical compound C1CCC2CCCC1[B]2 AMKGKYQBASDDJB-UHFFFAOYSA-N 0.000 description 21
FEJUGLKDZJDVFY-UHFFFAOYSA-N 9-borabicyclo[3.3.1]nonane Substances C1CCC2CCCC1B2 FEJUGLKDZJDVFY-UHFFFAOYSA-N 0.000 description 21
LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 19
QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
238000010348 incorporation Methods 0.000 description 18
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 17
QCIYAEYRVFUFAP-UHFFFAOYSA-N hexane-2,3-diol Chemical compound CCCC(O)C(C)O QCIYAEYRVFUFAP-UHFFFAOYSA-N 0.000 description 17
101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 16
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
239000002253 acid Substances 0.000 description 15
FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 15
238000012360 testing method Methods 0.000 description 15
239000012298 atmosphere Substances 0.000 description 14
239000002585 base Substances 0.000 description 14
239000003153 chemical reaction reagent Substances 0.000 description 14
NKLCNNUWBJBICK-UHFFFAOYSA-N dess–martin periodinane Chemical compound C1=CC=C2I(OC(=O)C)(OC(C)=O)(OC(C)=O)OC(=O)C2=C1 NKLCNNUWBJBICK-UHFFFAOYSA-N 0.000 description 14
239000000725 suspension Substances 0.000 description 14
KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 13
DHSMOJJTKZZRDX-UHFFFAOYSA-N 6ah-cyclopenta[d][1,3]dioxole Chemical compound C1=CC=C2OCOC21 DHSMOJJTKZZRDX-UHFFFAOYSA-N 0.000 description 13
238000006197 hydroboration reaction Methods 0.000 description 13
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 13
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 13
VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 12
125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 12
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 12
102000004190 Enzymes Human genes 0.000 description 12
108090000790 Enzymes Proteins 0.000 description 12
XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 12
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 12
238000010511 deprotection reaction Methods 0.000 description 12
229910052757 nitrogen Inorganic materials 0.000 description 12
229910052938 sodium sulfate Inorganic materials 0.000 description 12
235000011152 sodium sulphate Nutrition 0.000 description 12
239000002904 solvent Substances 0.000 description 12
FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 12
238000006069 Suzuki reaction reaction Methods 0.000 description 11
125000000446 sulfanediyl group Chemical group *S* 0.000 description 11
AWQSPXJCKUAANQ-UPJWGTAASA-N CC1(C)O[C@@H]2[C@H](O1)C(C=C)=C[C@H]2N1C=CC2=C1N=CN=C2Cl Chemical compound CC1(C)O[C@@H]2[C@H](O1)C(C=C)=C[C@H]2N1C=CC2=C1N=CN=C2Cl AWQSPXJCKUAANQ-UPJWGTAASA-N 0.000 description 10
GXHBPWSIARZMLO-MCIONIFRSA-N CC1=NC=NC2=C1C=CN2[C@@H]1C=C(C=O)[C@H]2OC(C)(C)O[C@@H]12 Chemical compound CC1=NC=NC2=C1C=CN2[C@@H]1C=C(C=O)[C@H]2OC(C)(C)O[C@@H]12 GXHBPWSIARZMLO-MCIONIFRSA-N 0.000 description 10
150000007513 acids Chemical class 0.000 description 10
125000001246 bromo group Chemical group Br* 0.000 description 10
229910000024 caesium carbonate Inorganic materials 0.000 description 10
125000005843 halogen group Chemical group 0.000 description 10
230000003647 oxidation Effects 0.000 description 10
238000007254 oxidation reaction Methods 0.000 description 10
VVWRJUBEIPHGQF-MDZDMXLPSA-N propan-2-yl (ne)-n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)\N=N\C(=O)OC(C)C VVWRJUBEIPHGQF-MDZDMXLPSA-N 0.000 description 10
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 9
KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 9
IUBQJLUDMLPAGT-UHFFFAOYSA-N potassium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([K])[Si](C)(C)C IUBQJLUDMLPAGT-UHFFFAOYSA-N 0.000 description 9
230000002829 reductive effect Effects 0.000 description 9
229940062627 tribasic potassium phosphate Drugs 0.000 description 9
239000003039 volatile agent Substances 0.000 description 9
NLEPLDKPYLYCSY-UHFFFAOYSA-N 2-fluoroquinoline Chemical compound C1=CC=CC2=NC(F)=CC=C21 NLEPLDKPYLYCSY-UHFFFAOYSA-N 0.000 description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
QWOJMRHUQHTCJG-UHFFFAOYSA-N CC([CH2-])=O Chemical compound CC([CH2-])=O QWOJMRHUQHTCJG-UHFFFAOYSA-N 0.000 description 8
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
235000019270 ammonium chloride Nutrition 0.000 description 8
230000015572 biosynthetic process Effects 0.000 description 8
239000012230 colorless oil Substances 0.000 description 8
238000001514 detection method Methods 0.000 description 8
238000001914 filtration Methods 0.000 description 8
150000007529 inorganic bases Chemical class 0.000 description 8
NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 8
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 8
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 8
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
238000002953 preparative HPLC Methods 0.000 description 8
SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical compound C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 8
239000003826 tablet Substances 0.000 description 8
NCZOVCDTUUZEEA-UHFFFAOYSA-N 3-methylquinolin-2-amine Chemical compound C1=CC=C2N=C(N)C(C)=CC2=C1 NCZOVCDTUUZEEA-UHFFFAOYSA-N 0.000 description 7
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
241001465754 Metazoa Species 0.000 description 7
239000002775 capsule Substances 0.000 description 7
239000003054 catalyst Substances 0.000 description 7
230000008878 coupling Effects 0.000 description 7
238000010168 coupling process Methods 0.000 description 7
238000005859 coupling reaction Methods 0.000 description 7
CRHWEIDCXNDTMO-UHFFFAOYSA-N ditert-butylphosphane Chemical compound CC(C)(C)PC(C)(C)C CRHWEIDCXNDTMO-UHFFFAOYSA-N 0.000 description 7
238000002868 homogeneous time resolved fluorescence Methods 0.000 description 7
230000002401 inhibitory effect Effects 0.000 description 7
239000000463 material Substances 0.000 description 7
LSEFCHWGJNHZNT-UHFFFAOYSA-M methyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 LSEFCHWGJNHZNT-UHFFFAOYSA-M 0.000 description 7
PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 7
239000000546 pharmaceutical excipient Substances 0.000 description 7
239000000758 substrate Substances 0.000 description 7
YJLIKUSWRSEPSM-WGQQHEPDSA-N (2r,3r,4s,5r)-2-[6-amino-8-[(4-phenylphenyl)methylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1CNC1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O YJLIKUSWRSEPSM-WGQQHEPDSA-N 0.000 description 6
GBBSAMQTQCPOBF-UHFFFAOYSA-N 2,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinane Chemical compound CB1OB(C)OB(C)O1 GBBSAMQTQCPOBF-UHFFFAOYSA-N 0.000 description 6
KGOVLLDJDHNNQZ-YWAHFTAISA-N ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1[C@@H]2[C@]([C@@H]3[C@H]1OC(O3)(C)C)(C2)C=C Chemical compound ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1[C@@H]2[C@]([C@@H]3[C@H]1OC(O3)(C)C)(C2)C=C KGOVLLDJDHNNQZ-YWAHFTAISA-N 0.000 description 6
238000006751 Mitsunobu reaction Methods 0.000 description 6
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 6
PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 6
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 6
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
125000005604 azodicarboxylate group Chemical group 0.000 description 6
UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical class B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 6
229910000085 borane Inorganic materials 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
125000003963 dichloro group Chemical group Cl* 0.000 description 6
BLEBFDYUDVZRFG-UHFFFAOYSA-N dichloromethane;propan-2-ol Chemical compound ClCCl.CC(C)O BLEBFDYUDVZRFG-UHFFFAOYSA-N 0.000 description 6
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 6
ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 6
239000013642 negative control Substances 0.000 description 6
229910000073 phosphorus hydride Inorganic materials 0.000 description 6
235000017557 sodium bicarbonate Nutrition 0.000 description 6
229910000030 sodium bicarbonate Inorganic materials 0.000 description 6
WRIKHQLVHPKCJU-UHFFFAOYSA-N sodium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([Na])[Si](C)(C)C WRIKHQLVHPKCJU-UHFFFAOYSA-N 0.000 description 6
125000003003 spiro group Chemical group 0.000 description 6
239000000126 substance Substances 0.000 description 6
238000003786 synthesis reaction Methods 0.000 description 6
229960000549 4-dimethylaminophenol Drugs 0.000 description 5
OWNHZWUZCJRCLH-UHFFFAOYSA-N BrC1=CC(=C2C=C(C(=NC2=C1)N)Cl)F Chemical compound BrC1=CC(=C2C=C(C(=NC2=C1)N)Cl)F OWNHZWUZCJRCLH-UHFFFAOYSA-N 0.000 description 5
241000699670 Mus sp. Species 0.000 description 5
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
125000003342 alkenyl group Chemical group 0.000 description 5
125000000304 alkynyl group Chemical group 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
125000004429 atom Chemical group 0.000 description 5
238000004296 chiral HPLC Methods 0.000 description 5
229940125904 compound 1 Drugs 0.000 description 5
125000006001 difluoroethyl group Chemical group 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000000706 filtrate Substances 0.000 description 5
239000005457 ice water Substances 0.000 description 5
239000002609 medium Substances 0.000 description 5
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 5
238000007069 methylation reaction Methods 0.000 description 5
MUJIDPITZJWBSW-UHFFFAOYSA-N palladium(2+) Chemical compound [Pd+2] MUJIDPITZJWBSW-UHFFFAOYSA-N 0.000 description 5
239000000047 product Substances 0.000 description 5
OYRRZWATULMEPF-UHFFFAOYSA-N pyrimidin-4-amine Chemical compound NC1=CC=NC=N1 OYRRZWATULMEPF-UHFFFAOYSA-N 0.000 description 5
229910000104 sodium hydride Inorganic materials 0.000 description 5
208000024891 symptom Diseases 0.000 description 5
DJMOXMNDXFFONV-UHFFFAOYSA-N 1,3-dimethyl-7-[2-(n-methylanilino)ethyl]purine-2,6-dione Chemical compound C1=NC=2N(C)C(=O)N(C)C(=O)C=2N1CCN(C)C1=CC=CC=C1 DJMOXMNDXFFONV-UHFFFAOYSA-N 0.000 description 4
KKHFRAFPESRGGD-UHFFFAOYSA-N 1,3-dimethyl-7-[3-(n-methylanilino)propyl]purine-2,6-dione Chemical compound C1=NC=2N(C)C(=O)N(C)C(=O)C=2N1CCCN(C)C1=CC=CC=C1 KKHFRAFPESRGGD-UHFFFAOYSA-N 0.000 description 4
UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 description 4
FQMZXMVHHKXGTM-UHFFFAOYSA-N 2-(1-adamantyl)-n-[2-[2-(2-hydroxyethylamino)ethylamino]quinolin-5-yl]acetamide Chemical compound C1C(C2)CC(C3)CC2CC13CC(=O)NC1=CC=CC2=NC(NCCNCCO)=CC=C21 FQMZXMVHHKXGTM-UHFFFAOYSA-N 0.000 description 4
PYRKKGOKRMZEIT-UHFFFAOYSA-N 2-[6-(2-cyclopropylethoxy)-9-(2-hydroxy-2-methylpropyl)-1h-phenanthro[9,10-d]imidazol-2-yl]-5-fluorobenzene-1,3-dicarbonitrile Chemical compound C1=C2C3=CC(CC(C)(O)C)=CC=C3C=3NC(C=4C(=CC(F)=CC=4C#N)C#N)=NC=3C2=CC=C1OCCC1CC1 PYRKKGOKRMZEIT-UHFFFAOYSA-N 0.000 description 4
DVEPYWNSVJBFRR-UHFFFAOYSA-N 2-amino-4-bromo-6-fluorobenzaldehyde Chemical compound Nc1cc(Br)cc(F)c1C=O DVEPYWNSVJBFRR-UHFFFAOYSA-N 0.000 description 4
MKEUDOGZIJGFJP-UHFFFAOYSA-N 2-cyclopropylquinoline Chemical compound C1CC1C1=CC=C(C=CC=C2)C2=N1 MKEUDOGZIJGFJP-UHFFFAOYSA-N 0.000 description 4
FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 4
QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 4
AUHHINKFSCQZIT-UHFFFAOYSA-N 3-bromo-7-iodo-N-[(4-methoxyphenyl)methyl]quinolin-2-amine Chemical compound COC1=CC=C(CNC2=C(Br)C=C3C=CC(I)=CC3=N2)C=C1 AUHHINKFSCQZIT-UHFFFAOYSA-N 0.000 description 4
PGSIGXRMGPKKTB-UHFFFAOYSA-N 3-chloroquinolin-2-amine Chemical compound C1=CC=C2C=C(Cl)C(N)=NC2=C1 PGSIGXRMGPKKTB-UHFFFAOYSA-N 0.000 description 4
LVQFHDAKZHGEAJ-UHFFFAOYSA-M 4-methylbenzenesulfonate Chemical compound [CH2]C1=CC=C(S([O-])(=O)=O)C=C1 LVQFHDAKZHGEAJ-UHFFFAOYSA-M 0.000 description 4
YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 4
POAHOBOVGAUBJG-UHFFFAOYSA-N 7-bromo-N-[(4-methoxyphenyl)methyl]quinolin-2-amine Chemical compound COC1=CC=C(CNC2=NC3=CC(Br)=CC=C3C=C2)C=C1 POAHOBOVGAUBJG-UHFFFAOYSA-N 0.000 description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
239000004475 Arginine Substances 0.000 description 4
JQUCWIWWWKZNCS-LESHARBVSA-N C(C1=CC=CC=C1)(=O)NC=1SC[C@H]2[C@@](N1)(CO[C@H](C2)C)C=2SC=C(N2)NC(=O)C2=NC=C(C=C2)OC(F)F Chemical compound C(C1=CC=CC=C1)(=O)NC=1SC[C@H]2[C@@](N1)(CO[C@H](C2)C)C=2SC=C(N2)NC(=O)C2=NC=C(C=C2)OC(F)F JQUCWIWWWKZNCS-LESHARBVSA-N 0.000 description 4
SULUETCFJPGNEQ-OAGGEKHMSA-N CC(=C)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2C Chemical compound CC(=C)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2C SULUETCFJPGNEQ-OAGGEKHMSA-N 0.000 description 4
PKMUHQIDVVOXHQ-HXUWFJFHSA-N C[C@H](C1=CC(C2=CC=C(CNC3CCCC3)S2)=CC=C1)NC(C1=C(C)C=CC(NC2CNC2)=C1)=O Chemical compound C[C@H](C1=CC(C2=CC=C(CNC3CCCC3)S2)=CC=C1)NC(C1=C(C)C=CC(NC2CNC2)=C1)=O PKMUHQIDVVOXHQ-HXUWFJFHSA-N 0.000 description 4
239000004215 Carbon black (E152) Substances 0.000 description 4
NHIZHSJKHLNPHU-UHFFFAOYSA-N ClC=1C(=NC2=CC(=CC(=C2C=1)F)O)NCC1=CC=C(C=C1)OC Chemical compound ClC=1C(=NC2=CC(=CC(=C2C=1)F)O)NCC1=CC=C(C=C1)OC NHIZHSJKHLNPHU-UHFFFAOYSA-N 0.000 description 4
108010010803 Gelatin Proteins 0.000 description 4
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-diisopropylethylamine Substances CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 4
229910021529 ammonia Inorganic materials 0.000 description 4
230000001093 anti-cancer Effects 0.000 description 4
ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 4
XRWSZZJLZRKHHD-WVWIJVSJSA-N asunaprevir Chemical compound O=C([C@@H]1C[C@H](CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)OC1=NC=C(C2=CC=C(Cl)C=C21)OC)N[C@]1(C(=O)NS(=O)(=O)C2CC2)C[C@H]1C=C XRWSZZJLZRKHHD-WVWIJVSJSA-N 0.000 description 4
239000000872 buffer Substances 0.000 description 4
150000001721 carbon Chemical group 0.000 description 4
229940125961 compound 24 Drugs 0.000 description 4
229940125846 compound 25 Drugs 0.000 description 4
229940127573 compound 38 Drugs 0.000 description 4
229940126179 compound 72 Drugs 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
CSJLBAMHHLJAAS-UHFFFAOYSA-N diethylaminosulfur trifluoride Chemical compound CCN(CC)S(F)(F)F CSJLBAMHHLJAAS-UHFFFAOYSA-N 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
239000002552 dosage form Substances 0.000 description 4
BJXYHBKEQFQVES-NWDGAFQWSA-N enpatoran Chemical compound N[C@H]1CN(C[C@H](C1)C(F)(F)F)C1=C2C=CC=NC2=C(C=C1)C#N BJXYHBKEQFQVES-NWDGAFQWSA-N 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
239000008273 gelatin Substances 0.000 description 4
229920000159 gelatin Polymers 0.000 description 4
235000019322 gelatine Nutrition 0.000 description 4
235000011852 gelatine desserts Nutrition 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
229910052740 iodine Inorganic materials 0.000 description 4
239000011630 iodine Substances 0.000 description 4
PIDFDZJZLOTZTM-KHVQSSSXSA-N ombitasvir Chemical compound COC(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)NC1=CC=C([C@H]2N([C@@H](CC2)C=2C=CC(NC(=O)[C@H]3N(CCC3)C(=O)[C@@H](NC(=O)OC)C(C)C)=CC=2)C=2C=CC(=CC=2)C(C)(C)C)C=C1 PIDFDZJZLOTZTM-KHVQSSSXSA-N 0.000 description 4
239000007800 oxidant agent Substances 0.000 description 4
239000006187 pill Substances 0.000 description 4
239000013641 positive control Substances 0.000 description 4
229910000027 potassium carbonate Inorganic materials 0.000 description 4
238000011160 research Methods 0.000 description 4
238000006467 substitution reaction Methods 0.000 description 4
229910000404 tripotassium phosphate Inorganic materials 0.000 description 4
235000019798 tripotassium phosphate Nutrition 0.000 description 4
230000004614 tumor growth Effects 0.000 description 4
239000003981 vehicle Substances 0.000 description 4
SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 3
IUSARDYWEPUTPN-OZBXUNDUSA-N (2r)-n-[(2s,3r)-4-[[(4s)-6-(2,2-dimethylpropyl)spiro[3,4-dihydropyrano[2,3-b]pyridine-2,1'-cyclobutane]-4-yl]amino]-3-hydroxy-1-[3-(1,3-thiazol-2-yl)phenyl]butan-2-yl]-2-methoxypropanamide Chemical compound C([C@H](NC(=O)[C@@H](C)OC)[C@H](O)CN[C@@H]1C2=CC(CC(C)(C)C)=CN=C2OC2(CCC2)C1)C(C=1)=CC=CC=1C1=NC=CS1 IUSARDYWEPUTPN-OZBXUNDUSA-N 0.000 description 3
UDQTXCHQKHIQMH-KYGLGHNPSA-N (3ar,5s,6s,7r,7ar)-5-(difluoromethyl)-2-(ethylamino)-5,6,7,7a-tetrahydro-3ah-pyrano[3,2-d][1,3]thiazole-6,7-diol Chemical compound S1C(NCC)=N[C@H]2[C@@H]1O[C@H](C(F)F)[C@@H](O)[C@@H]2O UDQTXCHQKHIQMH-KYGLGHNPSA-N 0.000 description 3
HUWSZNZAROKDRZ-RRLWZMAJSA-N (3r,4r)-3-azaniumyl-5-[[(2s,3r)-1-[(2s)-2,3-dicarboxypyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl]amino]-5-oxo-4-sulfanylpentane-1-sulfonate Chemical compound OS(=O)(=O)CC[C@@H](N)[C@@H](S)C(=O)N[C@@H]([C@H](C)CC)C(=O)N1CCC(C(O)=O)[C@H]1C(O)=O HUWSZNZAROKDRZ-RRLWZMAJSA-N 0.000 description 3
YQOLEILXOBUDMU-KRWDZBQOSA-N (4R)-5-[(6-bromo-3-methyl-2-pyrrolidin-1-ylquinoline-4-carbonyl)amino]-4-(2-chlorophenyl)pentanoic acid Chemical compound CC1=C(C2=C(C=CC(=C2)Br)N=C1N3CCCC3)C(=O)NC[C@H](CCC(=O)O)C4=CC=CC=C4Cl YQOLEILXOBUDMU-KRWDZBQOSA-N 0.000 description 3
GZTMCZAOQTVOJK-UHFFFAOYSA-N 1,3-dioxolan-4-one Chemical compound O=C1COCO1 GZTMCZAOQTVOJK-UHFFFAOYSA-N 0.000 description 3
KQZLRWGGWXJPOS-NLFPWZOASA-N 1-[(1R)-1-(2,4-dichlorophenyl)ethyl]-6-[(4S,5R)-4-[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-5-methylcyclohexen-1-yl]pyrazolo[3,4-b]pyrazine-3-carbonitrile Chemical compound ClC1=C(C=CC(=C1)Cl)[C@@H](C)N1N=C(C=2C1=NC(=CN=2)C1=CC[C@@H]([C@@H](C1)C)N1[C@@H](CCC1)CO)C#N KQZLRWGGWXJPOS-NLFPWZOASA-N 0.000 description 3
NRKYWOKHZRQRJR-UHFFFAOYSA-N 2,2,2-trifluoroacetamide Chemical compound NC(=O)C(F)(F)F NRKYWOKHZRQRJR-UHFFFAOYSA-N 0.000 description 3
IAZGSHMUMOEDDD-UHFFFAOYSA-N 2-(bromomethyl)-1-chloro-5-iodo-3-nitrobenzene Chemical compound [O-][N+](=O)c1cc(I)cc(Cl)c1CBr IAZGSHMUMOEDDD-UHFFFAOYSA-N 0.000 description 3
NXFFJDQHYLNEJK-UHFFFAOYSA-N 2-[4-[(4-chlorophenyl)methyl]-7-fluoro-5-methylsulfonyl-2,3-dihydro-1h-cyclopenta[b]indol-3-yl]acetic acid Chemical compound C1=2C(S(=O)(=O)C)=CC(F)=CC=2C=2CCC(CC(O)=O)C=2N1CC1=CC=C(Cl)C=C1 NXFFJDQHYLNEJK-UHFFFAOYSA-N 0.000 description 3
YSUIQYOGTINQIN-UZFYAQMZSA-N 2-amino-9-[(1S,6R,8R,9S,10R,15R,17R,18R)-8-(6-aminopurin-9-yl)-9,18-difluoro-3,12-dihydroxy-3,12-bis(sulfanylidene)-2,4,7,11,13,16-hexaoxa-3lambda5,12lambda5-diphosphatricyclo[13.2.1.06,10]octadecan-17-yl]-1H-purin-6-one Chemical compound NC1=NC2=C(N=CN2[C@@H]2O[C@@H]3COP(S)(=O)O[C@@H]4[C@@H](COP(S)(=O)O[C@@H]2[C@@H]3F)O[C@H]([C@H]4F)N2C=NC3=C2N=CN=C3N)C(=O)N1 YSUIQYOGTINQIN-UZFYAQMZSA-N 0.000 description 3
NPRYCHLHHVWLQZ-TURQNECASA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynylpurin-8-one Chemical compound NC1=NC=C2N(C(N(C2=N1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C NPRYCHLHHVWLQZ-TURQNECASA-N 0.000 description 3
FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 description 3
ZTQNUTNKGQGWCM-UHFFFAOYSA-N 2-methoxyquinoline Chemical compound C1=CC=CC2=NC(OC)=CC=C21 ZTQNUTNKGQGWCM-UHFFFAOYSA-N 0.000 description 3
ZQGOVWFEPPTLAF-UHFFFAOYSA-N 3-bromo-N-[(4-methoxyphenyl)methyl]-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine Chemical compound COC1=CC=C(CNC2=NC3=CC(=CC=C3C=C2Br)B2OC(C)(C)C(C)(C)O2)C=C1 ZQGOVWFEPPTLAF-UHFFFAOYSA-N 0.000 description 3
UZOVYGYOLBIAJR-UHFFFAOYSA-N 4-isocyanato-4'-methyldiphenylmethane Chemical compound C1=CC(C)=CC=C1CC1=CC=C(N=C=O)C=C1 UZOVYGYOLBIAJR-UHFFFAOYSA-N 0.000 description 3
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
DSYBMAAUKWLGEI-UHFFFAOYSA-N BrC1=CC(=C2C=C(C=NC2=C1)Cl)F Chemical compound BrC1=CC(=C2C=C(C=NC2=C1)Cl)F DSYBMAAUKWLGEI-UHFFFAOYSA-N 0.000 description 3
YXOWETLXNOVHEP-UHFFFAOYSA-N BrC1=CC=C2C(C(NC2=C1)=S)(C)C Chemical compound BrC1=CC=C2C(C(NC2=C1)=S)(C)C YXOWETLXNOVHEP-UHFFFAOYSA-N 0.000 description 3
VGLQLFJGVXMTHW-UHFFFAOYSA-N BrC=1C(=NC2=CC(=CC=C2C=1)O)NCC1=CC=C(C=C1)OC Chemical compound BrC=1C(=NC2=CC(=CC=C2C=1)O)NCC1=CC=C(C=C1)OC VGLQLFJGVXMTHW-UHFFFAOYSA-N 0.000 description 3
OOWHAGPUXLCFHQ-UPJWGTAASA-N CC(=O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl Chemical compound CC(=O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl OOWHAGPUXLCFHQ-UPJWGTAASA-N 0.000 description 3
MJRMBBCJZQPWIR-YWAHFTAISA-N CC1(C)O[C@@H]2[C@H](O1)[C@@]1(C[C@@H]1[C@H]2n1ccc2c(N)ncnc12)C=C Chemical compound CC1(C)O[C@@H]2[C@H](O1)[C@@]1(C[C@@H]1[C@H]2n1ccc2c(N)ncnc12)C=C MJRMBBCJZQPWIR-YWAHFTAISA-N 0.000 description 3
208000005623 Carcinogenesis Diseases 0.000 description 3
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 3
UTAYNUGOKJFTJZ-UHFFFAOYSA-N ClC=1C(=NC2=CC=CC(=C2C=1)F)N Chemical compound ClC=1C(=NC2=CC=CC(=C2C=1)F)N UTAYNUGOKJFTJZ-UHFFFAOYSA-N 0.000 description 3
ZFLKELDSPLIFNF-UTUOFQBUSA-N ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)C=O Chemical compound ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)C=O ZFLKELDSPLIFNF-UTUOFQBUSA-N 0.000 description 3
PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 3
108020004414 DNA Proteins 0.000 description 3
108010033040 Histones Proteins 0.000 description 3
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
LQZMLBORDGWNPD-UHFFFAOYSA-N N-iodosuccinimide Substances IN1C(=O)CCC1=O LQZMLBORDGWNPD-UHFFFAOYSA-N 0.000 description 3
LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 description 3
OPFJDXRVMFKJJO-ZHHKINOHSA-N N-{[3-(2-benzamido-4-methyl-1,3-thiazol-5-yl)-pyrazol-5-yl]carbonyl}-G-dR-G-dD-dD-dD-NH2 Chemical compound S1C(C=2NN=C(C=2)C(=O)NCC(=O)N[C@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(N)=O)=C(C)N=C1NC(=O)C1=CC=CC=C1 OPFJDXRVMFKJJO-ZHHKINOHSA-N 0.000 description 3
239000007832 Na2SO4 Substances 0.000 description 3
108700020796 Oncogene Proteins 0.000 description 3
229910002666 PdCl2 Inorganic materials 0.000 description 3
229920001213 Polysorbate 20 Polymers 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
238000007239 Wittig reaction Methods 0.000 description 3
LJOOWESTVASNOG-UFJKPHDISA-N [(1s,3r,4ar,7s,8s,8as)-3-hydroxy-8-[2-[(4r)-4-hydroxy-6-oxooxan-2-yl]ethyl]-7-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl] (2s)-2-methylbutanoate Chemical compound C([C@H]1[C@@H](C)C=C[C@H]2C[C@@H](O)C[C@@H]([C@H]12)OC(=O)[C@@H](C)CC)CC1C[C@@H](O)CC(=O)O1 LJOOWESTVASNOG-UFJKPHDISA-N 0.000 description 3
LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 3
230000009471 action Effects 0.000 description 3
238000003556 assay Methods 0.000 description 3
230000008901 benefit Effects 0.000 description 3
KGNDCEVUMONOKF-UGPLYTSKSA-N benzyl n-[(2r)-1-[(2s,4r)-2-[[(2s)-6-amino-1-(1,3-benzoxazol-2-yl)-1,1-dihydroxyhexan-2-yl]carbamoyl]-4-[(4-methylphenyl)methoxy]pyrrolidin-1-yl]-1-oxo-4-phenylbutan-2-yl]carbamate Chemical compound C1=CC(C)=CC=C1CO[C@H]1CN(C(=O)[C@@H](CCC=2C=CC=CC=2)NC(=O)OCC=2C=CC=CC=2)[C@H](C(=O)N[C@@H](CCCCN)C(O)(O)C=2OC3=CC=CC=C3N=2)C1 KGNDCEVUMONOKF-UGPLYTSKSA-N 0.000 description 3
230000036952 cancer formation Effects 0.000 description 3
125000002837 carbocyclic group Chemical group 0.000 description 3
231100000504 carcinogenesis Toxicity 0.000 description 3
230000003833 cell viability Effects 0.000 description 3
230000001413 cellular effect Effects 0.000 description 3
239000007910 chewable tablet Substances 0.000 description 3
229940126543 compound 14 Drugs 0.000 description 3
229940125782 compound 2 Drugs 0.000 description 3
229940126086 compound 21 Drugs 0.000 description 3
229940125833 compound 23 Drugs 0.000 description 3
229940127204 compound 29 Drugs 0.000 description 3
229940125877 compound 31 Drugs 0.000 description 3
229940125807 compound 37 Drugs 0.000 description 3
229940126540 compound 41 Drugs 0.000 description 3
229940125936 compound 42 Drugs 0.000 description 3
229940125844 compound 46 Drugs 0.000 description 3
239000012043 crude product Substances 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 description 3
238000005516 engineering process Methods 0.000 description 3
238000002347 injection Methods 0.000 description 3
239000007924 injection Substances 0.000 description 3
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
RENRQMCACQEWFC-UGKGYDQZSA-N lnp023 Chemical compound C1([C@H]2N(CC=3C=4C=CNC=4C(C)=CC=3OC)CC[C@@H](C2)OCC)=CC=C(C(O)=O)C=C1 RENRQMCACQEWFC-UGKGYDQZSA-N 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
230000011987 methylation Effects 0.000 description 3
IOMMMLWIABWRKL-WUTDNEBXSA-N nazartinib Chemical compound C1N(C(=O)/C=C/CN(C)C)CCCC[C@H]1N1C2=C(Cl)C=CC=C2N=C1NC(=O)C1=CC=NC(C)=C1 IOMMMLWIABWRKL-WUTDNEBXSA-N 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
229910000069 nitrogen hydride Inorganic materials 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
JOXIMZWYDAKGHI-UHFFFAOYSA-N p-toluenesulfonic acid Substances CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
125000006684 polyhaloalkyl group Polymers 0.000 description 3
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 3
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
125000006239 protecting group Chemical group 0.000 description 3
108090000623 proteins and genes Proteins 0.000 description 3
102000004169 proteins and genes Human genes 0.000 description 3
230000001696 purinergic effect Effects 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
238000004007 reversed phase HPLC Methods 0.000 description 3
230000011664 signaling Effects 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
238000004809 thin layer chromatography Methods 0.000 description 3
ASGMFNBUXDJWJJ-JLCFBVMHSA-N (1R,3R)-3-[[3-bromo-1-[4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]pyrazolo[3,4-d]pyrimidin-6-yl]amino]-N,1-dimethylcyclopentane-1-carboxamide Chemical compound BrC1=NN(C2=NC(=NC=C21)N[C@H]1C[C@@](CC1)(C(=O)NC)C)C1=CC=C(C=C1)C=1SC(=NN=1)C ASGMFNBUXDJWJJ-JLCFBVMHSA-N 0.000 description 2
UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 description 2
PPXHIEAORXNBNC-MZYLBHOOSA-N (1S,2R,5R)-3-[2-(2-amino-3-chloro-5-fluoroquinolin-7-yl)ethyl]-5-(4-cyclopropylpyrrolo[2,3-d]pyrimidin-7-yl)cyclopent-3-ene-1,2-diol Chemical compound NC1=NC2=CC(CCC3=C[C@H]([C@H](O)[C@@H]3O)N3C=CC4=C3N=CN=C4C3CC3)=CC(F)=C2C=C1Cl PPXHIEAORXNBNC-MZYLBHOOSA-N 0.000 description 2
AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 description 2
GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 2
VIJSPAIQWVPKQZ-BLECARSGSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-acetamido-5-(diaminomethylideneamino)pentanoyl]amino]-4-methylpentanoyl]amino]-4,4-dimethylpentanoyl]amino]-4-methylpentanoyl]amino]propanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid Chemical compound NC(=N)NCCC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(N)=N)NC(C)=O VIJSPAIQWVPKQZ-BLECARSGSA-N 0.000 description 2
QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 2
FNHHVPPSBFQMEL-KQHDFZBMSA-N (3S)-5-N-[(1S,5R)-3-hydroxy-6-bicyclo[3.1.0]hexanyl]-7-N,3-dimethyl-3-phenyl-2H-1-benzofuran-5,7-dicarboxamide Chemical compound CNC(=O)c1cc(cc2c1OC[C@@]2(C)c1ccccc1)C(=O)NC1[C@H]2CC(O)C[C@@H]12 FNHHVPPSBFQMEL-KQHDFZBMSA-N 0.000 description 2
IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 2
OOKAZRDERJMRCJ-KOUAFAAESA-N (3r)-7-[(1s,2s,4ar,6s,8s)-2,6-dimethyl-8-[(2s)-2-methylbutanoyl]oxy-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-3-hydroxy-5-oxoheptanoic acid Chemical compound C1=C[C@H](C)[C@H](CCC(=O)C[C@@H](O)CC(O)=O)C2[C@@H](OC(=O)[C@@H](C)CC)C[C@@H](C)C[C@@H]21 OOKAZRDERJMRCJ-KOUAFAAESA-N 0.000 description 2
MPDDTAJMJCESGV-CTUHWIOQSA-M (3r,5r)-7-[2-(4-fluorophenyl)-5-[methyl-[(1r)-1-phenylethyl]carbamoyl]-4-propan-2-ylpyrazol-3-yl]-3,5-dihydroxyheptanoate Chemical compound C1([C@@H](C)N(C)C(=O)C2=NN(C(CC[C@@H](O)C[C@@H](O)CC([O-])=O)=C2C(C)C)C=2C=CC(F)=CC=2)=CC=CC=C1 MPDDTAJMJCESGV-CTUHWIOQSA-M 0.000 description 2
STPKWKPURVSAJF-LJEWAXOPSA-N (4r,5r)-5-[4-[[4-(1-aza-4-azoniabicyclo[2.2.2]octan-4-ylmethyl)phenyl]methoxy]phenyl]-3,3-dibutyl-7-(dimethylamino)-1,1-dioxo-4,5-dihydro-2h-1$l^{6}-benzothiepin-4-ol Chemical compound O[C@H]1C(CCCC)(CCCC)CS(=O)(=O)C2=CC=C(N(C)C)C=C2[C@H]1C(C=C1)=CC=C1OCC(C=C1)=CC=C1C[N+]1(CC2)CCN2CC1 STPKWKPURVSAJF-LJEWAXOPSA-N 0.000 description 2
DEVSOMFAQLZNKR-RJRFIUFISA-N (z)-3-[3-[3,5-bis(trifluoromethyl)phenyl]-1,2,4-triazol-1-yl]-n'-pyrazin-2-ylprop-2-enehydrazide Chemical compound FC(F)(F)C1=CC(C(F)(F)F)=CC(C2=NN(\C=C/C(=O)NNC=3N=CC=NC=3)C=N2)=C1 DEVSOMFAQLZNKR-RJRFIUFISA-N 0.000 description 2
LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 description 2
VRTZOIPOBBAYPL-UHFFFAOYSA-N 1,3-dioxole-4-carbaldehyde Chemical compound O=CC1=COCO1 VRTZOIPOBBAYPL-UHFFFAOYSA-N 0.000 description 2
WZZBNLYBHUDSHF-DHLKQENFSA-N 1-[(3s,4s)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone Chemical compound CC1=NC2=CN=C3C=C(F)C(C=4C(=CC(OC=5N=CC=CN=5)=CC=4)Cl)=CC3=C2N1[C@H]1CCN(C(=O)CO)C[C@@H]1F WZZBNLYBHUDSHF-DHLKQENFSA-N 0.000 description 2
ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 2
MLODDQGSENCNJU-UHFFFAOYSA-N 1-chloro-5-iodo-2-methyl-3-nitrobenzene Chemical compound Cc1c(Cl)cc(I)cc1[N+]([O-])=O MLODDQGSENCNJU-UHFFFAOYSA-N 0.000 description 2
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
WGFNXGPBPIJYLI-UHFFFAOYSA-N 2,6-difluoro-3-[(3-fluorophenyl)sulfonylamino]-n-(3-methoxy-1h-pyrazolo[3,4-b]pyridin-5-yl)benzamide Chemical compound C1=C2C(OC)=NNC2=NC=C1NC(=O)C(C=1F)=C(F)C=CC=1NS(=O)(=O)C1=CC=CC(F)=C1 WGFNXGPBPIJYLI-UHFFFAOYSA-N 0.000 description 2
FMKGJQHNYMWDFJ-CVEARBPZSA-N 2-[[4-(2,2-difluoropropoxy)pyrimidin-5-yl]methylamino]-4-[[(1R,4S)-4-hydroxy-3,3-dimethylcyclohexyl]amino]pyrimidine-5-carbonitrile Chemical compound FC(COC1=NC=NC=C1CNC1=NC=C(C(=N1)N[C@H]1CC([C@H](CC1)O)(C)C)C#N)(C)F FMKGJQHNYMWDFJ-CVEARBPZSA-N 0.000 description 2
VVCMGAUPZIKYTH-VGHSCWAPSA-N 2-acetyloxybenzoic acid;[(2s,3r)-4-(dimethylamino)-3-methyl-1,2-diphenylbutan-2-yl] propanoate;1,3,7-trimethylpurine-2,6-dione Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O.CN1C(=O)N(C)C(=O)C2=C1N=CN2C.C([C@](OC(=O)CC)([C@H](C)CN(C)C)C=1C=CC=CC=1)C1=CC=CC=C1 VVCMGAUPZIKYTH-VGHSCWAPSA-N 0.000 description 2
ZZVUOSVSPAPBEJ-UHFFFAOYSA-N 2-amino-4-bromobenzaldehyde Chemical compound NC1=CC(Br)=CC=C1C=O ZZVUOSVSPAPBEJ-UHFFFAOYSA-N 0.000 description 2
TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 2
ZWDVQMVZZYIAHO-UHFFFAOYSA-N 2-fluorobenzaldehyde Chemical compound FC1=CC=CC=C1C=O ZWDVQMVZZYIAHO-UHFFFAOYSA-N 0.000 description 2
WWKKTHALZAYYAI-UHFFFAOYSA-N 2-iodobenzaldehyde Chemical compound IC1=CC=CC=C1C=O WWKKTHALZAYYAI-UHFFFAOYSA-N 0.000 description 2
LFOIDLOIBZFWDO-UHFFFAOYSA-N 2-methoxy-6-[6-methoxy-4-[(3-phenylmethoxyphenyl)methoxy]-1-benzofuran-2-yl]imidazo[2,1-b][1,3,4]thiadiazole Chemical compound N1=C2SC(OC)=NN2C=C1C(OC1=CC(OC)=C2)=CC1=C2OCC(C=1)=CC=CC=1OCC1=CC=CC=C1 LFOIDLOIBZFWDO-UHFFFAOYSA-N 0.000 description 2
DFRAKBCRUYUFNT-UHFFFAOYSA-N 3,8-dicyclohexyl-2,4,7,9-tetrahydro-[1,3]oxazino[5,6-h][1,3]benzoxazine Chemical compound C1CCCCC1N1CC(C=CC2=C3OCN(C2)C2CCCCC2)=C3OC1 DFRAKBCRUYUFNT-UHFFFAOYSA-N 0.000 description 2
NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 2
WYFCZWSWFGJODV-MIANJLSGSA-N 4-[[(1s)-2-[(e)-3-[3-chloro-2-fluoro-6-(tetrazol-1-yl)phenyl]prop-2-enoyl]-5-(4-methyl-2-oxopiperazin-1-yl)-3,4-dihydro-1h-isoquinoline-1-carbonyl]amino]benzoic acid Chemical compound O=C1CN(C)CCN1C1=CC=CC2=C1CCN(C(=O)\C=C\C=1C(=CC=C(Cl)C=1F)N1N=NN=C1)[C@@H]2C(=O)NC1=CC=C(C(O)=O)C=C1 WYFCZWSWFGJODV-MIANJLSGSA-N 0.000 description 2
VNHBYKHXBCYPBJ-UHFFFAOYSA-N 5-ethynylimidazo[1,2-a]pyridine Chemical compound C#CC1=CC=CC2=NC=CN12 VNHBYKHXBCYPBJ-UHFFFAOYSA-N 0.000 description 2
RSIWALKZYXPAGW-NSHDSACASA-N 6-(3-fluorophenyl)-3-methyl-7-[(1s)-1-(7h-purin-6-ylamino)ethyl]-[1,3]thiazolo[3,2-a]pyrimidin-5-one Chemical compound C=1([C@@H](NC=2C=3N=CNC=3N=CN=2)C)N=C2SC=C(C)N2C(=O)C=1C1=CC=CC(F)=C1 RSIWALKZYXPAGW-NSHDSACASA-N 0.000 description 2
GDUANFXPOZTYKS-UHFFFAOYSA-N 6-bromo-8-[(2,6-difluoro-4-methoxybenzoyl)amino]-4-oxochromene-2-carboxylic acid Chemical compound FC1=CC(OC)=CC(F)=C1C(=O)NC1=CC(Br)=CC2=C1OC(C(O)=O)=CC2=O GDUANFXPOZTYKS-UHFFFAOYSA-N 0.000 description 2
HCCNBKFJYUWLEX-UHFFFAOYSA-N 7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)-3-(pyrazin-2-ylmethylamino)pyrido[3,4-b]pyrazin-2-one Chemical compound O=C1N(CCOCCC)C2=CC(C=3C=NC(OC)=CC=3)=NC=C2N=C1NCC1=CN=CC=N1 HCCNBKFJYUWLEX-UHFFFAOYSA-N 0.000 description 2
KSFQTOOWTKNZEL-UHFFFAOYSA-N 7-bromo-3-chloroquinolin-2-amine Chemical compound BrC1=CC=C2C=C(C(=NC2=C1)N)Cl KSFQTOOWTKNZEL-UHFFFAOYSA-N 0.000 description 2
IDDWGXXNSVIXOH-UHFFFAOYSA-N 7-bromo-N-propan-2-ylquinolin-2-amine Chemical compound CC(C)NC1=NC2=CC(Br)=CC=C2C=C1 IDDWGXXNSVIXOH-UHFFFAOYSA-N 0.000 description 2
PEHVGBZKEYRQSX-UHFFFAOYSA-N 7-deaza-adenine Chemical compound NC1=NC=NC2=C1C=CN2 PEHVGBZKEYRQSX-UHFFFAOYSA-N 0.000 description 2
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
JKJBQZCVQUFBKD-UHFFFAOYSA-N BrC1=CC(=C2C=C(C(=NC2=C1)Cl)Cl)F Chemical compound BrC1=CC(=C2C=C(C(=NC2=C1)Cl)Cl)F JKJBQZCVQUFBKD-UHFFFAOYSA-N 0.000 description 2
SGYSIEHJHSWNQV-UHFFFAOYSA-N BrC1=CC(=C2C=C(C=[N+](C2=C1)[O-])Cl)F Chemical compound BrC1=CC(=C2C=C(C=[N+](C2=C1)[O-])Cl)F SGYSIEHJHSWNQV-UHFFFAOYSA-N 0.000 description 2
LDJDUORCXGEEFL-UHFFFAOYSA-N BrC1=CC=C2C(C(=NC2=C1)SC)(C)C Chemical compound BrC1=CC=C2C(C(=NC2=C1)SC)(C)C LDJDUORCXGEEFL-UHFFFAOYSA-N 0.000 description 2
WDZRBHDCYDPMMC-UHFFFAOYSA-N BrC1=CC=C2C=C(C=NC2=C1)C1CC1 Chemical compound BrC1=CC=C2C=C(C=NC2=C1)C1CC1 WDZRBHDCYDPMMC-UHFFFAOYSA-N 0.000 description 2
IVDLSWCLXKRNSR-UHFFFAOYSA-N BrC=1C(=NC2=CC(=CC(=C2C=1)F)Br)N Chemical compound BrC=1C(=NC2=CC(=CC(=C2C=1)F)Br)N IVDLSWCLXKRNSR-UHFFFAOYSA-N 0.000 description 2
AFOCUOYTKOLLDC-UHFFFAOYSA-N C1(CCC1)C=1C(=NC2=CC=CC=C2C=1)N Chemical compound C1(CCC1)C=1C(=NC2=CC=CC=C2C=1)N AFOCUOYTKOLLDC-UHFFFAOYSA-N 0.000 description 2
OJRUSAPKCPIVBY-KQYNXXCUSA-N C1=NC2=C(N=C(N=C2N1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(CP(=O)(O)O)O)O)O)I)N Chemical compound C1=NC2=C(N=C(N=C2N1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(CP(=O)(O)O)O)O)O)I)N OJRUSAPKCPIVBY-KQYNXXCUSA-N 0.000 description 2
GGHHNCAZIQKASU-UPJWGTAASA-N CC(C)(O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl Chemical compound CC(C)(O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl GGHHNCAZIQKASU-UPJWGTAASA-N 0.000 description 2
PLVTYBHAEWDJFN-HIRWBNPYSA-N CC(O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl Chemical compound CC(O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl PLVTYBHAEWDJFN-HIRWBNPYSA-N 0.000 description 2
VYGNZDVBKILFQG-ZOUHWKOYSA-N CC1(C)O[C@@H]2[C@H](O1)[C@@]1(C[C@@H]1[C@H]2n1ccc2c(Cl)ncnc12)C=O Chemical compound CC1(C)O[C@@H]2[C@H](O1)[C@@]1(C[C@@H]1[C@H]2n1ccc2c(Cl)ncnc12)C=O VYGNZDVBKILFQG-ZOUHWKOYSA-N 0.000 description 2
IBSCRWGLOKACBH-UHFFFAOYSA-N CNC1=NC2=CC(=CC=C2C=C1)O Chemical compound CNC1=NC2=CC(=CC=C2C=C1)O IBSCRWGLOKACBH-UHFFFAOYSA-N 0.000 description 2
GBCOAWMFDMQEQH-UHFFFAOYSA-N COC1=CC=C(CNC2=NC3=CC(=CC=C3C=C2)N)C=C1 Chemical compound COC1=CC=C(CNC2=NC3=CC(=CC=C3C=C2)N)C=C1 GBCOAWMFDMQEQH-UHFFFAOYSA-N 0.000 description 2
JWBPMKVQZSOKFK-UHFFFAOYSA-N COC1=CC=C(CNC2=NC3=CC(=CC=C3C=C2)NC)C=C1 Chemical compound COC1=CC=C(CNC2=NC3=CC(=CC=C3C=C2)NC)C=C1 JWBPMKVQZSOKFK-UHFFFAOYSA-N 0.000 description 2
WROVCLYRQBZRNC-UHFFFAOYSA-N COC1=CC=C(CNC2=NC3=CC(=CC=C3C=C2)S)C=C1 Chemical compound COC1=CC=C(CNC2=NC3=CC(=CC=C3C=C2)S)C=C1 WROVCLYRQBZRNC-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
102100025064 Cellular tumor antigen p53 Human genes 0.000 description 2
XKKQWKWUGFNCES-UHFFFAOYSA-N ClC1=C(C=O)C(=CC(=C1)I)[N+](=O)[O-] Chemical compound ClC1=C(C=O)C(=CC(=C1)I)[N+](=O)[O-] XKKQWKWUGFNCES-UHFFFAOYSA-N 0.000 description 2
229940126657 Compound 17 Drugs 0.000 description 2
229940127007 Compound 39 Drugs 0.000 description 2
241000689227 Cora <basidiomycete fungus> Species 0.000 description 2
OKKJLVBELUTLKV-MZCSYVLQSA-N Deuterated methanol Chemical compound [2H]OC([2H])([2H])[2H] OKKJLVBELUTLKV-MZCSYVLQSA-N 0.000 description 2
101000693916 Gallus gallus Albumin Proteins 0.000 description 2
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical group NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
101000582546 Homo sapiens Methylosome protein 50 Proteins 0.000 description 2
101000757232 Homo sapiens Protein arginine N-methyltransferase 2 Proteins 0.000 description 2
241000124008 Mammalia Species 0.000 description 2
102100030528 Methylosome protein 50 Human genes 0.000 description 2
241000699666 Mus <mouse, genus> Species 0.000 description 2
101100521345 Mus musculus Prop1 gene Proteins 0.000 description 2
FSVCELGFZIQNCK-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)glycine Chemical compound OCCN(CCO)CC(O)=O FSVCELGFZIQNCK-UHFFFAOYSA-N 0.000 description 2
150000001204 N-oxides Chemical class 0.000 description 2
QOVYHDHLFPKQQG-NDEPHWFRSA-N N[C@@H](CCC(=O)N1CCC(CC1)NC1=C2C=CC=CC2=NC(NCC2=CN(CCCNCCCNC3CCCCC3)N=N2)=N1)C(O)=O Chemical compound N[C@@H](CCC(=O)N1CCC(CC1)NC1=C2C=CC=CC2=NC(NCC2=CN(CCCNCCCNC3CCCCC3)N=N2)=N1)C(O)=O QOVYHDHLFPKQQG-NDEPHWFRSA-N 0.000 description 2
206010031112 Oropharyngeal squamous cell carcinoma Diseases 0.000 description 2
241000283973 Oryctolagus cuniculus Species 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
108700017836 Prophet of Pit-1 Proteins 0.000 description 2
108020000912 Protein arginine N-methyltransferase Proteins 0.000 description 2
102000003708 Protein arginine N-methyltransferase Human genes 0.000 description 2
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
208000000102 Squamous Cell Carcinoma of Head and Neck Diseases 0.000 description 2
229910000831 Steel Inorganic materials 0.000 description 2
SPXSEZMVRJLHQG-XMMPIXPASA-N [(2R)-1-[[4-[(3-phenylmethoxyphenoxy)methyl]phenyl]methyl]pyrrolidin-2-yl]methanol Chemical compound C(C1=CC=CC=C1)OC=1C=C(OCC2=CC=C(CN3[C@H](CCC3)CO)C=C2)C=CC=1 SPXSEZMVRJLHQG-XMMPIXPASA-N 0.000 description 2
IOSLINNLJFQMFF-XMMPIXPASA-N [(2R)-1-[[4-[[3-[(4-fluorophenyl)methylsulfanyl]phenoxy]methyl]phenyl]methyl]pyrrolidin-2-yl]methanol Chemical compound FC1=CC=C(CSC=2C=C(OCC3=CC=C(CN4[C@H](CCC4)CO)C=C3)C=CC=2)C=C1 IOSLINNLJFQMFF-XMMPIXPASA-N 0.000 description 2
238000002835 absorbance Methods 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
239000008186 active pharmaceutical agent Substances 0.000 description 2
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
208000016063 arterial thoracic outlet syndrome Diseases 0.000 description 2
239000012131 assay buffer Substances 0.000 description 2
CBHOOMGKXCMKIR-UHFFFAOYSA-N azane;methanol Chemical compound N.OC CBHOOMGKXCMKIR-UHFFFAOYSA-N 0.000 description 2
HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
239000007998 bicine buffer Substances 0.000 description 2
238000010256 biochemical assay Methods 0.000 description 2
238000010876 biochemical test Methods 0.000 description 2
YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 2
RMIBJVUYNZSLSD-UHFFFAOYSA-N bis[(1,1,1,3,3,3-hexafluoro-2-phenylpropan-2-yl)oxy]-diphenyl-$l^{4}-sulfane Chemical compound C=1C=CC=CC=1C(C(F)(F)F)(C(F)(F)F)OS(C=1C=CC=CC=1)(C=1C=CC=CC=1)OC(C(F)(F)F)(C(F)(F)F)C1=CC=CC=C1 RMIBJVUYNZSLSD-UHFFFAOYSA-N 0.000 description 2
239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
229910002091 carbon monoxide Inorganic materials 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
230000004663 cell proliferation Effects 0.000 description 2
238000005660 chlorination reaction Methods 0.000 description 2
WBLIXGSTEMXDSM-UHFFFAOYSA-N chloromethane Chemical compound Cl[CH2] WBLIXGSTEMXDSM-UHFFFAOYSA-N 0.000 description 2
229940125773 compound 10 Drugs 0.000 description 2
229940125797 compound 12 Drugs 0.000 description 2
229940125758 compound 15 Drugs 0.000 description 2
229940126142 compound 16 Drugs 0.000 description 2
229940126208 compound 22 Drugs 0.000 description 2
229940125851 compound 27 Drugs 0.000 description 2
229940126214 compound 3 Drugs 0.000 description 2
229940127271 compound 49 Drugs 0.000 description 2
229940125898 compound 5 Drugs 0.000 description 2
229940126545 compound 53 Drugs 0.000 description 2
229940127113 compound 57 Drugs 0.000 description 2
229940125900 compound 59 Drugs 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
235000008504 concentrate Nutrition 0.000 description 2
239000007822 coupling agent Substances 0.000 description 2
LMKPHJYTFHAGHK-UHFFFAOYSA-N cyclodrine Chemical compound C1CCCC1(O)C(C(=O)OCCN(CC)CC)C1=CC=CC=C1 LMKPHJYTFHAGHK-UHFFFAOYSA-N 0.000 description 2
230000018044 dehydration Effects 0.000 description 2
238000006297 dehydration reaction Methods 0.000 description 2
238000011161 development Methods 0.000 description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
229950010286 diolamine Drugs 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
239000001963 growth medium Substances 0.000 description 2
102000046485 human PRMT2 Human genes 0.000 description 2
238000001990 intravenous administration Methods 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 2
208000032839 leukemia Diseases 0.000 description 2
238000012417 linear regression Methods 0.000 description 2
YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 2
238000004020 luminiscence type Methods 0.000 description 2
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
229910052943 magnesium sulfate Inorganic materials 0.000 description 2
235000019341 magnesium sulphate Nutrition 0.000 description 2
108010082117 matrigel Proteins 0.000 description 2
230000001404 mediated effect Effects 0.000 description 2
108020004999 messenger RNA Proteins 0.000 description 2
ZBELDPMWYXDLNY-UHFFFAOYSA-N methyl 9-(4-bromo-2-fluoroanilino)-[1,3]thiazolo[5,4-f]quinazoline-2-carboximidate Chemical compound C12=C3SC(C(=N)OC)=NC3=CC=C2N=CN=C1NC1=CC=C(Br)C=C1F ZBELDPMWYXDLNY-UHFFFAOYSA-N 0.000 description 2
239000002808 molecular sieve Substances 0.000 description 2
125000002950 monocyclic group Chemical group 0.000 description 2
125000006682 monohaloalkyl group Chemical group 0.000 description 2
VQSRKMNBWMHJKY-YTEVENLXSA-N n-[3-[(4ar,7as)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-5-methoxypyrazine-2-carboxamide Chemical compound C1=NC(OC)=CN=C1C(=O)NC1=CC=C(F)C([C@@]23[C@@H](CN(C2)C=2N=CC(F)=CN=2)CSC(N)=N3)=C1 VQSRKMNBWMHJKY-YTEVENLXSA-N 0.000 description 2
YGBMCLDVRUGXOV-UHFFFAOYSA-N n-[6-[6-chloro-5-[(4-fluorophenyl)sulfonylamino]pyridin-3-yl]-1,3-benzothiazol-2-yl]acetamide Chemical compound C1=C2SC(NC(=O)C)=NC2=CC=C1C(C=1)=CN=C(Cl)C=1NS(=O)(=O)C1=CC=C(F)C=C1 YGBMCLDVRUGXOV-UHFFFAOYSA-N 0.000 description 2
239000012299 nitrogen atmosphere Substances 0.000 description 2
125000006574 non-aromatic ring group Chemical group 0.000 description 2
238000010534 nucleophilic substitution reaction Methods 0.000 description 2
208000022698 oropharynx squamous cell carcinoma Diseases 0.000 description 2
KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
235000015320 potassium carbonate Nutrition 0.000 description 2
235000011181 potassium carbonates Nutrition 0.000 description 2
239000000843 powder Substances 0.000 description 2
LEHBURLTIWGHEM-UHFFFAOYSA-N pyridinium chlorochromate Chemical compound [O-][Cr](Cl)(=O)=O.C1=CC=[NH+]C=C1 LEHBURLTIWGHEM-UHFFFAOYSA-N 0.000 description 2
QZZYYBQGTSGDPP-UHFFFAOYSA-N quinoline-3-carbonitrile Chemical compound C1=CC=CC2=CC(C#N)=CN=C21 QZZYYBQGTSGDPP-UHFFFAOYSA-N 0.000 description 2
125000005493 quinolyl group Chemical group 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
239000012279 sodium borohydride Substances 0.000 description 2
229910000033 sodium borohydride Inorganic materials 0.000 description 2
239000012312 sodium hydride Substances 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 2
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
235000019345 sodium thiosulphate Nutrition 0.000 description 2
HJDSVSUVQHFMSM-UHFFFAOYSA-N spiro[cyclobutane-1,3'-indole]-2'-amine Chemical compound NC1=NC2=CC=CC=C2C11CCC1 HJDSVSUVQHFMSM-UHFFFAOYSA-N 0.000 description 2
239000010959 steel Substances 0.000 description 2
238000007920 subcutaneous administration Methods 0.000 description 2
239000000454 talc Substances 0.000 description 2
235000012222 talc Nutrition 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
125000004568 thiomorpholinyl group Chemical group 0.000 description 2
210000001519 tissue Anatomy 0.000 description 2
230000000699 topical effect Effects 0.000 description 2
230000037426 transcriptional repression Effects 0.000 description 2
238000013519 translation Methods 0.000 description 2
230000032258 transport Effects 0.000 description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 2
GNLJBJNONOOOQC-UHFFFAOYSA-N $l^{3}-carbane;magnesium Chemical compound [Mg]C GNLJBJNONOOOQC-UHFFFAOYSA-N 0.000 description 1
VEEGVNVWQSORRN-QEVAIPBGSA-N (1S,2R,5R)-3-[1-(2-amino-3-chloro-5-fluoroquinolin-7-yl)propan-2-yl]-2-methyl-5-(4-methylpyrrolo[2,3-d]pyrimidin-7-yl)cyclopent-3-ene-1,2-diol Chemical compound NC1=NC2=CC(=CC(=C2C=C1Cl)F)CC(C)C=1[C@]([C@H]([C@@H](C=1)N1C=CC2=C1N=CN=C2C)O)(O)C VEEGVNVWQSORRN-QEVAIPBGSA-N 0.000 description 1
CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 1
LJIOTBMDLVHTBO-CUYJMHBOSA-N (2s)-2-amino-n-[(1r,2r)-1-cyano-2-[4-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]phenyl]cyclopropyl]butanamide Chemical compound CC[C@H](N)C(=O)N[C@]1(C#N)C[C@@H]1C1=CC=C(C=2C=CC(=CC=2)S(=O)(=O)N2CCN(C)CC2)C=C1 LJIOTBMDLVHTBO-CUYJMHBOSA-N 0.000 description 1
ZCWNYVGRWFQRCL-JKIFEVAISA-N (3aR,6R,6aS)-2,2,3a-trimethyl-6-(4-methylpyrrolo[2,3-d]pyrimidin-7-yl)-6,6a-dihydrocyclopenta[d][1,3]dioxole-4-carbaldehyde Chemical compound CC1(O[C@]2(C)C(=C[C@@H](N3C4=NC=NC(=C4C=C3)C)[C@@H]2O1)C=O)C ZCWNYVGRWFQRCL-JKIFEVAISA-N 0.000 description 1
VUDZSIYXZUYWSC-DBRKOABJSA-N (4r)-1-[(2r,4r,5r)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-hydroxy-1,3-diazinan-2-one Chemical compound FC1(F)[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)N[C@H](O)CC1 VUDZSIYXZUYWSC-DBRKOABJSA-N 0.000 description 1
FRJJJAKBRKABFA-TYFAACHXSA-N (4r,6s)-6-[(e)-2-[6-chloro-4-(4-fluorophenyl)-2-propan-2-ylquinolin-3-yl]ethenyl]-4-hydroxyoxan-2-one Chemical compound C(\[C@H]1OC(=O)C[C@H](O)C1)=C/C=1C(C(C)C)=NC2=CC=C(Cl)C=C2C=1C1=CC=C(F)C=C1 FRJJJAKBRKABFA-TYFAACHXSA-N 0.000 description 1
FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical compound C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 description 1
WMKGGPCROCCUDY-UHFFFAOYSA-N 1,5-diphenylpenta-1,4-dien-3-one Chemical compound C=1C=CC=CC=1C=CC(=O)C=CC1=CC=CC=C1 WMKGGPCROCCUDY-UHFFFAOYSA-N 0.000 description 1
IDPURXSQCKYKIJ-UHFFFAOYSA-N 1-(4-methoxyphenyl)methanamine Chemical compound COC1=CC=C(CN)C=C1 IDPURXSQCKYKIJ-UHFFFAOYSA-N 0.000 description 1
LYQOPNMWQZTJHA-UHFFFAOYSA-N 1-(7-bromoquinolin-3-yl)ethanone Chemical compound C1=C(Br)C=CC2=CC(C(=O)C)=CN=C21 LYQOPNMWQZTJHA-UHFFFAOYSA-N 0.000 description 1
IWRXLJHPSSHCIY-UHFFFAOYSA-N 1-(bromomethyl)-5-fluoro-4-iodo-2-nitrobenzene Chemical compound [O-][N+](=O)c1cc(I)c(F)cc1CBr IWRXLJHPSSHCIY-UHFFFAOYSA-N 0.000 description 1
MOHYOXXOKFQHDC-UHFFFAOYSA-N 1-(chloromethyl)-4-methoxybenzene Chemical compound COC1=CC=C(CCl)C=C1 MOHYOXXOKFQHDC-UHFFFAOYSA-N 0.000 description 1
125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
DPEVXZFONRKZFU-UHFFFAOYSA-N 1-fluoro-2-iodo-5-methyl-4-nitrobenzene Chemical compound CC1=CC(F)=C(I)C=C1[N+]([O-])=O DPEVXZFONRKZFU-UHFFFAOYSA-N 0.000 description 1
XBIAGSJDARBSKG-UHFFFAOYSA-N 1-hydroxypyrrole Chemical compound ON1C=CC=C1 XBIAGSJDARBSKG-UHFFFAOYSA-N 0.000 description 1
YRNQYNOHFVVGOE-UHFFFAOYSA-M 1-iodoethyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C(I)C)C1=CC=CC=C1 YRNQYNOHFVVGOE-UHFFFAOYSA-M 0.000 description 1
MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 1
125000006017 1-propenyl group Chemical group 0.000 description 1
AZUCPFMKPGFGTB-UHFFFAOYSA-N 2,2-diiodopropane Chemical compound CC(C)(I)I AZUCPFMKPGFGTB-UHFFFAOYSA-N 0.000 description 1
GPWNWKWQOLEVEQ-UHFFFAOYSA-N 2,4-diaminopyrimidine-5-carbaldehyde Chemical compound NC1=NC=C(C=O)C(N)=N1 GPWNWKWQOLEVEQ-UHFFFAOYSA-N 0.000 description 1
JYWKEVKEKOTYEX-UHFFFAOYSA-N 2,6-dibromo-4-chloroiminocyclohexa-2,5-dien-1-one Chemical compound ClN=C1C=C(Br)C(=O)C(Br)=C1 JYWKEVKEKOTYEX-UHFFFAOYSA-N 0.000 description 1
GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
CRZJPEIBPQWDGJ-UHFFFAOYSA-N 2-chloro-1,1-dimethoxyethane Chemical compound COC(CCl)OC CRZJPEIBPQWDGJ-UHFFFAOYSA-N 0.000 description 1
XCSNRORTQRKCHB-UHFFFAOYSA-N 2-chloro-6-nitrotoluene Chemical compound CC1=C(Cl)C=CC=C1[N+]([O-])=O XCSNRORTQRKCHB-UHFFFAOYSA-N 0.000 description 1
HJOQGBBHVRYTDX-UHFFFAOYSA-N 2-chloro-7h-pyrrolo[2,3-d]pyrimidine Chemical compound ClC1=NC=C2C=CNC2=N1 HJOQGBBHVRYTDX-UHFFFAOYSA-N 0.000 description 1
CSPMWYOOKWBXRI-UHFFFAOYSA-N 2-chloro-8-fluoroquinoline Chemical compound C1=C(Cl)N=C2C(F)=CC=CC2=C1 CSPMWYOOKWBXRI-UHFFFAOYSA-N 0.000 description 1
OFUFXTHGZWIDDB-UHFFFAOYSA-N 2-chloroquinoline Chemical compound C1=CC=CC2=NC(Cl)=CC=C21 OFUFXTHGZWIDDB-UHFFFAOYSA-N 0.000 description 1
TUHIBIVYQLRGME-UHFFFAOYSA-N 2-cyclopropylacetaldehyde Chemical compound O=CCC1CC1 TUHIBIVYQLRGME-UHFFFAOYSA-N 0.000 description 1
CZPWVGJYEJSRLH-QYKNYGDISA-N 2-deuteriopyrimidine Chemical compound [2H]C1=NC=CC=N1 CZPWVGJYEJSRLH-QYKNYGDISA-N 0.000 description 1
OUNUNDAIKLDJAY-UHFFFAOYSA-N 2-fluoro-4-methyl-5-nitroaniline Chemical compound CC1=CC(F)=C(N)C=C1[N+]([O-])=O OUNUNDAIKLDJAY-UHFFFAOYSA-N 0.000 description 1
125000006020 2-methyl-1-propenyl group Chemical group 0.000 description 1
ZHXISMXDCUJVCY-UHFFFAOYSA-N 2-phenylsulfanylethanamine;hydrochloride Chemical compound [Cl-].[NH3+]CCSC1=CC=CC=C1 ZHXISMXDCUJVCY-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
GSSXLFACIJSBOM-UHFFFAOYSA-N 2h-pyran-2-ol Chemical compound OC1OC=CC=C1 GSSXLFACIJSBOM-UHFFFAOYSA-N 0.000 description 1
UAIUNKRWKOVEES-UHFFFAOYSA-N 3,3',5,5'-tetramethylbenzidine Chemical compound CC1=C(N)C(C)=CC(C=2C=C(C)C(N)=C(C)C=2)=C1 UAIUNKRWKOVEES-UHFFFAOYSA-N 0.000 description 1
CDVAIHNNWWJFJW-UHFFFAOYSA-N 3,5-diethoxycarbonyl-1,4-dihydrocollidine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C CDVAIHNNWWJFJW-UHFFFAOYSA-N 0.000 description 1
VGOALPIDEXVYQI-UHFFFAOYSA-N 3-(2-imidazo[1,2-b]pyridazin-3-ylethynyl)-n-[3-imidazol-1-yl-5-(trifluoromethyl)phenyl]-4-methylbenzamide Chemical compound C1=C(C#CC=2N3N=CC=CC3=NC=2)C(C)=CC=C1C(=O)NC(C=C(C=1)C(F)(F)F)=CC=1N1C=CN=C1 VGOALPIDEXVYQI-UHFFFAOYSA-N 0.000 description 1
UNSHMXUHOHBLIQ-UHFFFAOYSA-N 3-[4-chloro-3-(2-methylphenoxy)naphthalen-1-yl]-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione Chemical compound ClC1=C(C=C(C2=CC=CC=C12)N1C(NC(=CC1=O)C(F)(F)F)=O)OC1=C(C=CC=C1)C UNSHMXUHOHBLIQ-UHFFFAOYSA-N 0.000 description 1
HQDFUEWXUQVYCO-UHFFFAOYSA-N 3-bromo-5-fluoroquinolin-2-amine Chemical compound NC1=NC2=C(C=C1Br)C(F)=CC=C2 HQDFUEWXUQVYCO-UHFFFAOYSA-N 0.000 description 1
125000003974 3-carbamimidamidopropyl group Chemical group C(N)(=N)NCCC* 0.000 description 1
QCCNVSYMWHRRBZ-UHFFFAOYSA-N 3-chloro-5-fluoro-N-[(4-methoxyphenyl)methyl]-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine Chemical compound COC1=CC=C(CNC2=NC3=CC(=CC(F)=C3C=C2Cl)B2OC(C)(C)C(C)(C)O2)C=C1 QCCNVSYMWHRRBZ-UHFFFAOYSA-N 0.000 description 1
BAAAAZIWPXKOMB-UHFFFAOYSA-N 3-chloro-6-fluoroquinolin-2-amine Chemical compound NC1=NC2=C(C=C(F)C=C2)C=C1Cl BAAAAZIWPXKOMB-UHFFFAOYSA-N 0.000 description 1
PFBAJSSHQYFZEE-UHFFFAOYSA-N 3-cyclopropylquinolin-2-amine Chemical compound C1(CC1)C=1C(=NC2=CC=CC=C2C1)N PFBAJSSHQYFZEE-UHFFFAOYSA-N 0.000 description 1
NDQXBRCPYKGVED-UHFFFAOYSA-N 3-iodoquinoline Chemical compound C1=CC=CC2=CC(I)=CN=C21 NDQXBRCPYKGVED-UHFFFAOYSA-N 0.000 description 1
TWGSZWLZNYKIEF-UHFFFAOYSA-N 3-methoxyquinolin-2-amine Chemical compound C1=CC=C2N=C(N)C(OC)=CC2=C1 TWGSZWLZNYKIEF-UHFFFAOYSA-N 0.000 description 1
LCQFQPAVZHDKIG-UHFFFAOYSA-N 3-propan-2-ylquinolin-2-amine Chemical compound C1=CC=C2N=C(N)C(C(C)C)=CC2=C1 LCQFQPAVZHDKIG-UHFFFAOYSA-N 0.000 description 1
IKIBCVVUGNCJEZ-UHFFFAOYSA-N 4-bromo-2-fluoro-6-nitrobenzaldehyde Chemical compound [O-][N+](=O)c1cc(Br)cc(F)c1C=O IKIBCVVUGNCJEZ-UHFFFAOYSA-N 0.000 description 1
NGRAFQOJLPCUNE-UHFFFAOYSA-N 4-chloro-1h-pyrrolo[3,2-c]pyridine Chemical compound ClC1=NC=CC2=C1C=CN2 NGRAFQOJLPCUNE-UHFFFAOYSA-N 0.000 description 1
OOBFPXOXHUBRDN-UHFFFAOYSA-N 4-chloro-5-fluoro-7h-pyrrolo[2,3-d]pyrimidine Chemical compound C1=NC(Cl)=C2C(F)=CNC2=N1 OOBFPXOXHUBRDN-UHFFFAOYSA-N 0.000 description 1
HMZRBLDCDIXBAP-NWBBNIOWSA-N 4-chloro-7-[(1R,2S,4S,5R,6S)-2-ethenyl-8,8-dimethyl-7,9-dioxatricyclo[4.3.0.02,4]nonan-5-yl]-6-methylpyrrolo[2,3-d]pyrimidine Chemical compound ClC=1C2=C(N=CN=1)N(C(=C2)C)[C@@H]1[C@@H]2[C@]([C@@H]3[C@H]1OC(O3)(C)C)(C2)C=C HMZRBLDCDIXBAP-NWBBNIOWSA-N 0.000 description 1
LBUNNMJLXWQQBY-UHFFFAOYSA-N 4-fluorophenylboronic acid Chemical compound OB(O)C1=CC=C(F)C=C1 LBUNNMJLXWQQBY-UHFFFAOYSA-N 0.000 description 1
125000005986 4-piperidonyl group Chemical group 0.000 description 1
PRRZCLRTCFWQFI-UHFFFAOYSA-N 4-propan-2-yl-7h-pyrrolo[2,3-d]pyrimidine Chemical compound CC(C)C1=NC=NC2=C1C=CN2 PRRZCLRTCFWQFI-UHFFFAOYSA-N 0.000 description 1
HFYWOOUKPVJGBA-UHFFFAOYSA-N 4-propan-2-ylquinoline Chemical compound C1=CC=C2C(C(C)C)=CC=NC2=C1 HFYWOOUKPVJGBA-UHFFFAOYSA-N 0.000 description 1
ZXJUGAOBVOUBLB-UHFFFAOYSA-N 5,6,7,8-tetrahydro-4h-chromene Chemical compound C1C=COC2=C1CCCC2 ZXJUGAOBVOUBLB-UHFFFAOYSA-N 0.000 description 1
XFJBGINZIMNZBW-CRAIPNDOSA-N 5-chloro-2-[4-[(1r,2s)-2-[2-(5-methylsulfonylpyridin-2-yl)oxyethyl]cyclopropyl]piperidin-1-yl]pyrimidine Chemical compound N1=CC(S(=O)(=O)C)=CC=C1OCC[C@H]1[C@@H](C2CCN(CC2)C=2N=CC(Cl)=CN=2)C1 XFJBGINZIMNZBW-CRAIPNDOSA-N 0.000 description 1
FIWARHXVBSGQNJ-UHFFFAOYSA-N 5-fluoro-4-iodo-2-nitrobenzaldehyde Chemical compound [O-][N+](=O)c1cc(I)c(F)cc1C=O FIWARHXVBSGQNJ-UHFFFAOYSA-N 0.000 description 1
WMFXCDGQRHJFKL-UHFFFAOYSA-N 5-fluoroquinoline Chemical compound C1=CC=C2C(F)=CC=CC2=N1 WMFXCDGQRHJFKL-UHFFFAOYSA-N 0.000 description 1
DBAOYNGOQUASPE-UHFFFAOYSA-N 6-bromo-3,3-dimethyl-1h-indol-2-one Chemical compound BrC1=CC=C2C(C)(C)C(=O)NC2=C1 DBAOYNGOQUASPE-UHFFFAOYSA-N 0.000 description 1
DSROYDXRWJWKRT-UHFFFAOYSA-N 6-fluoroquinolin-2-amine Chemical compound C1=C(F)C=CC2=NC(N)=CC=C21 DSROYDXRWJWKRT-UHFFFAOYSA-N 0.000 description 1
HZGQCCSFFAPMKJ-UHFFFAOYSA-N 6-fluoroquinoline Chemical compound N1=C=CC=C2[CH]C(F)=CC=C21 HZGQCCSFFAPMKJ-UHFFFAOYSA-N 0.000 description 1
GRUOUJLVEHTOSW-UHFFFAOYSA-N 6-methyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine Chemical compound N1=C(N)N=C2NC(C)=CC2=C1N GRUOUJLVEHTOSW-UHFFFAOYSA-N 0.000 description 1
MFHUDWWESDXERH-UHFFFAOYSA-N 6aH-cyclopenta[d][1,3]dioxol-6-amine Chemical compound O1COC2C1=CC=C2N MFHUDWWESDXERH-UHFFFAOYSA-N 0.000 description 1
PFYWZFOILLEVRH-UHFFFAOYSA-N 7-bromo-2-chloro-3-propan-2-ylquinoline Chemical compound C1=C(Br)C=C2N=C(Cl)C(C(C)C)=CC2=C1 PFYWZFOILLEVRH-UHFFFAOYSA-N 0.000 description 1
MBSARWOAEFKWQM-UHFFFAOYSA-N 7-bromo-2-chloro-8-fluoroquinoline Chemical compound C1=C(Cl)N=C2C(F)=C(Br)C=CC2=C1 MBSARWOAEFKWQM-UHFFFAOYSA-N 0.000 description 1
WIORTZMYDLZJIG-UHFFFAOYSA-N 7-bromo-3-fluoroquinolin-2-amine Chemical compound NC1=NC2=CC(Br)=CC=C2C=C1F WIORTZMYDLZJIG-UHFFFAOYSA-N 0.000 description 1
CVFAZFPZYNGXHK-UHFFFAOYSA-N 7-bromo-3-methylquinoline Chemical compound C1=C(Br)C=CC2=CC(C)=CN=C21 CVFAZFPZYNGXHK-UHFFFAOYSA-N 0.000 description 1
QXKAZGUVDWLARG-UHFFFAOYSA-N 7-bromo-8-fluoroquinoline Chemical compound C1=CN=C2C(F)=C(Br)C=CC2=C1 QXKAZGUVDWLARG-UHFFFAOYSA-N 0.000 description 1
WJYLXXIPEWIILC-UHFFFAOYSA-N 7-bromo-N-(cyclopropylmethyl)quinolin-2-amine Chemical compound BrC1=CC=C2C=CC(=NC2=C1)NCC1CC1 WJYLXXIPEWIILC-UHFFFAOYSA-N 0.000 description 1
XIGILMFUXPAUDC-UHFFFAOYSA-N 7-bromo-N-[(4-methoxyphenyl)methyl]quinazolin-2-amine Chemical compound COC1=CC=C(CNC2=NC=C3C=CC(Br)=CC3=N2)C=C1 XIGILMFUXPAUDC-UHFFFAOYSA-N 0.000 description 1
OPSSIGFDINIIDY-UHFFFAOYSA-N 7-bromo-N-cyclobutylquinolin-2-amine Chemical compound BrC1=CC=C2C=CC(NC3CCC3)=NC2=C1 OPSSIGFDINIIDY-UHFFFAOYSA-N 0.000 description 1
QEAYLYXHQWVAOF-UHFFFAOYSA-N 7-bromo-n-methylquinolin-2-amine Chemical compound C1=CC(Br)=CC2=NC(NC)=CC=C21 QEAYLYXHQWVAOF-UHFFFAOYSA-N 0.000 description 1
VKPJHDQCHZUELB-UHFFFAOYSA-N 7-bromoquinolin-2-amine Chemical compound C1=CC(Br)=CC2=NC(N)=CC=C21 VKPJHDQCHZUELB-UHFFFAOYSA-N 0.000 description 1
LDIOUQIXNSSOGU-UHFFFAOYSA-N 8-(3-pentylamino)-2-methyl-3-(2-chloro-4-methoxyphenyl)-6,7-dihydro-5h-cyclopenta[d]pyrazolo[1,5-a]pyrimidine Chemical compound CC1=NN2C(NC(CC)CC)=C3CCCC3=NC2=C1C1=CC=C(OC)C=C1Cl LDIOUQIXNSSOGU-UHFFFAOYSA-N 0.000 description 1
206010000830 Acute leukaemia Diseases 0.000 description 1
241001103870 Adia Species 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
229920000856 Amylose Polymers 0.000 description 1
244000099147 Ananas comosus Species 0.000 description 1
235000007119 Ananas comosus Nutrition 0.000 description 1
101100220074 Arabidopsis thaliana CDA8 gene Proteins 0.000 description 1
AXXLAOYVJJFFKW-UHFFFAOYSA-N B1CCCCCCCC1C1CCCCCCCC1 Chemical compound B1CCCCCCCC1C1CCCCCCCC1 AXXLAOYVJJFFKW-UHFFFAOYSA-N 0.000 description 1
KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
KMBGFKTYDITZTF-UHFFFAOYSA-N BrC1=C(C=C2C=C(C=[N+](C2=C1)[O-])Cl)F Chemical compound BrC1=C(C=C2C=C(C=[N+](C2=C1)[O-])Cl)F KMBGFKTYDITZTF-UHFFFAOYSA-N 0.000 description 1
DPBGJMIWQLZHRA-UHFFFAOYSA-N BrC1=CC=C2C(NC(=S)C22CCC2)=C1 Chemical compound BrC1=CC=C2C(NC(=S)C22CCC2)=C1 DPBGJMIWQLZHRA-UHFFFAOYSA-N 0.000 description 1
NDONKSAGSFUFRU-UHFFFAOYSA-N BrC1=CC=C2C=C(C(=NC2=C1)N(CC1=CC=C(C=C1)OC)CC1=CC=C(C=C1)OC)Cl Chemical compound BrC1=CC=C2C=C(C(=NC2=C1)N(CC1=CC=C(C=C1)OC)CC1=CC=C(C=C1)OC)Cl NDONKSAGSFUFRU-UHFFFAOYSA-N 0.000 description 1
GYJNTOIQFSFCML-UHFFFAOYSA-N BrC1=CC=C2C=C(C(=NC2=C1)NCC1=CC=C(C=C1)OC)Cl Chemical compound BrC1=CC=C2C=C(C(=NC2=C1)NCC1=CC=C(C=C1)OC)Cl GYJNTOIQFSFCML-UHFFFAOYSA-N 0.000 description 1
JHRCLADRFHZLGC-UHFFFAOYSA-N BrC1=CC=C2C=C(C(=NC2=C1F)N)Cl Chemical compound BrC1=CC=C2C=C(C(=NC2=C1F)N)Cl JHRCLADRFHZLGC-UHFFFAOYSA-N 0.000 description 1
GKVJMNYKAOOFLF-UHFFFAOYSA-N BrC1=CC=C2C=C(C=NC2=C1F)Cl Chemical compound BrC1=CC=C2C=C(C=NC2=C1F)Cl GKVJMNYKAOOFLF-UHFFFAOYSA-N 0.000 description 1
FSCHNZKOKGAERF-UHFFFAOYSA-N BrC1=CC=C2C=C(C=[N+](C2=C1F)[O-])Cl Chemical compound BrC1=CC=C2C=C(C=[N+](C2=C1F)[O-])Cl FSCHNZKOKGAERF-UHFFFAOYSA-N 0.000 description 1
OMIAFUMLSAXMIF-UHFFFAOYSA-N BrC1=CC=C2C=CC(=NC2=C1F)N Chemical compound BrC1=CC=C2C=CC(=NC2=C1F)N OMIAFUMLSAXMIF-UHFFFAOYSA-N 0.000 description 1
MKVQAFMLLJVECH-NLDZOOGBSA-N BrC=1C(=NC2=CC(=CC=C2C=1)CCC1=C[C@H]([C@H]2[C@@H]1OC(O2)(C)C)N1C=CC2=C1N=CN=C2Cl)NCC1=CC=C(C=C1)OC Chemical compound BrC=1C(=NC2=CC(=CC=C2C=1)CCC1=C[C@H]([C@H]2[C@@H]1OC(O2)(C)C)N1C=CC2=C1N=CN=C2Cl)NCC1=CC=C(C=C1)OC MKVQAFMLLJVECH-NLDZOOGBSA-N 0.000 description 1
FMRWJHQVFXZQOX-UHFFFAOYSA-N BrC=1C=[N+](C2=CC(=CC(=C2C=1)F)Br)[O-] Chemical compound BrC=1C=[N+](C2=CC(=CC(=C2C=1)F)Br)[O-] FMRWJHQVFXZQOX-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
BCZRFLIOTGNCLD-UHFFFAOYSA-N C(C)(SC1=CC=C2C=CC(=NC2=C1)NCC1=CC=C(C=C1)OC)=O Chemical compound C(C)(SC1=CC=C2C=CC(=NC2=C1)NCC1=CC=C(C=C1)OC)=O BCZRFLIOTGNCLD-UHFFFAOYSA-N 0.000 description 1
OFZPGIDZDFRTBV-OIISXLGYSA-N C1(CC1)C=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)C=C Chemical compound C1(CC1)C=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)C=C OFZPGIDZDFRTBV-OIISXLGYSA-N 0.000 description 1
WWKARKXJLINUCU-ZOHTZWGFSA-N C1(O[C@@H]2C(=C[C@@H](N3C4=NC=NC(=C4C=C3)Cl)[C@@H]2O1)C(OC1=CC=C2C=CC(=NC2=C1)NC)C)(C)C Chemical compound C1(O[C@@H]2C(=C[C@@H](N3C4=NC=NC(=C4C=C3)Cl)[C@@H]2O1)C(OC1=CC=C2C=CC(=NC2=C1)NC)C)(C)C WWKARKXJLINUCU-ZOHTZWGFSA-N 0.000 description 1
VXVLCOBFMUTDGD-IIYDPXPESA-N C1(O[C@@]2(C(=C[C@@H](N3C4=NC=NC(=C4C=C3)Cl)[C@@H]2O1)C(=O)C)C)(C)C Chemical compound C1(O[C@@]2(C(=C[C@@H](N3C4=NC=NC(=C4C=C3)Cl)[C@@H]2O1)C(=O)C)C)(C)C VXVLCOBFMUTDGD-IIYDPXPESA-N 0.000 description 1
YCPVBTPYFWTXHX-MCIONIFRSA-N CC(=C)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl Chemical compound CC(=C)C1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl YCPVBTPYFWTXHX-MCIONIFRSA-N 0.000 description 1
VYTQGPWFUBFAFW-SWAFEPEESA-N CC(=O)[C@@]12C[C@@H]1[C@H]([C@@H]1OC(C)(C)O[C@H]21)n1ccc2c(Cl)ncnc12 Chemical compound CC(=O)[C@@]12C[C@@H]1[C@H]([C@@H]1OC(C)(C)O[C@H]21)n1ccc2c(Cl)ncnc12 VYTQGPWFUBFAFW-SWAFEPEESA-N 0.000 description 1
AXLMEYOIMNCVED-UHFFFAOYSA-N CC(C)c1cc2ccc(Br)cc2nc1N Chemical compound CC(C)c1cc2ccc(Br)cc2nc1N AXLMEYOIMNCVED-UHFFFAOYSA-N 0.000 description 1
RBMYLYADQCBSBW-OTUBZARLSA-N CC(CC1=CC(F)=C2C=C(Cl)C(N)=NC2=C1)C1=C[C@H]([C@H](O)[C@@H]1O)N1C=CC2=C1N=CN=C2N Chemical compound CC(CC1=CC(F)=C2C=C(Cl)C(N)=NC2=C1)C1=C[C@H]([C@H](O)[C@@H]1O)N1C=CC2=C1N=CN=C2N RBMYLYADQCBSBW-OTUBZARLSA-N 0.000 description 1
ROAPSBBDVNYWRO-UHFFFAOYSA-N CC(CC=C1)(C1O)O Chemical compound CC(CC=C1)(C1O)O ROAPSBBDVNYWRO-UHFFFAOYSA-N 0.000 description 1
QXWFQLUQZZBXAD-UHFFFAOYSA-N CC(F)(F)C1=CC2=CC=C(Br)C=C2N=C1 Chemical compound CC(F)(F)C1=CC2=CC=C(Br)C=C2N=C1 QXWFQLUQZZBXAD-UHFFFAOYSA-N 0.000 description 1
OWMOZQJQXYPNFM-UHFFFAOYSA-N CC(F)(F)c1cc2ccc(Br)cc2nc1N Chemical compound CC(F)(F)c1cc2ccc(Br)cc2nc1N OWMOZQJQXYPNFM-UHFFFAOYSA-N 0.000 description 1
FVAKTWLEKKPODQ-AWFZIKENSA-N CC(O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@]12C)N1C=CC2=C1N=CN=C2Cl Chemical compound CC(O)C1=C[C@H]([C@@H]2OC(C)(C)O[C@]12C)N1C=CC2=C1N=CN=C2Cl FVAKTWLEKKPODQ-AWFZIKENSA-N 0.000 description 1
JIUMQZKXKNBPTN-KFWWJZLASA-N CC1(C)O[C@@H]2[C@H](O1)C(C=C)=C[C@H]2N1C=CC2=C(Cl)N=CC=C12 Chemical compound CC1(C)O[C@@H]2[C@H](O1)C(C=C)=C[C@H]2N1C=CC2=C(Cl)N=CC=C12 JIUMQZKXKNBPTN-KFWWJZLASA-N 0.000 description 1
KACVVTMGQJUNGS-OAGGEKHMSA-N CC1(C)O[C@@H]2[C@H](O1)C(C=C)=C[C@H]2N1C=CC2=CN=CC=C12 Chemical compound CC1(C)O[C@@H]2[C@H](O1)C(C=C)=C[C@H]2N1C=CC2=CN=CC=C12 KACVVTMGQJUNGS-OAGGEKHMSA-N 0.000 description 1
KSXSWOMOORTPKT-UPJWGTAASA-N CC1(C)O[C@@H]2[C@H](O1)C(C=O)=C[C@H]2N1C=CC2=C1N=CN=C2 Chemical compound CC1(C)O[C@@H]2[C@H](O1)C(C=O)=C[C@H]2N1C=CC2=C1N=CN=C2 KSXSWOMOORTPKT-UPJWGTAASA-N 0.000 description 1
ZENXTEBYSOIDNJ-NJYVYQBISA-N CC1(C)O[C@@H]2[C@H](O1)C(CCC1=CC(F)=C3C=C(Cl)C(N)=NC3=C1)=C[C@H]2N1C=CC2=C1N=CN=C2Cl Chemical compound CC1(C)O[C@@H]2[C@H](O1)C(CCC1=CC(F)=C3C=C(Cl)C(N)=NC3=C1)=C[C@H]2N1C=CC2=C1N=CN=C2Cl ZENXTEBYSOIDNJ-NJYVYQBISA-N 0.000 description 1
NGXOBVCKSWXDBW-BFQNTYOBSA-N CC1(C)O[C@H]2[C@@H](C=C(C=O)[C@@]2(C)O1)N1C=CC2=C1N=CN=C2Cl Chemical compound CC1(C)O[C@H]2[C@@H](C=C(C=O)[C@@]2(C)O1)N1C=CC2=C1N=CN=C2Cl NGXOBVCKSWXDBW-BFQNTYOBSA-N 0.000 description 1
MPZBLGFRGGMIOI-NJYVYQBISA-N CC1(C)O[C@H]2[C@@H](C=C(CCC3=CC=C4C=C(F)C(N)=NC4=C3)[C@H]2O1)N1C=CC2=C1N=CN=C2N Chemical compound CC1(C)O[C@H]2[C@@H](C=C(CCC3=CC=C4C=C(F)C(N)=NC4=C3)[C@H]2O1)N1C=CC2=C1N=CN=C2N MPZBLGFRGGMIOI-NJYVYQBISA-N 0.000 description 1
QYMUYMVEYDKDDH-RTXFEEFZSA-N CC1(O[C@@H]2C(=C[C@@H](N3C4=NC=NC(=C4C(=C3)F)Cl)[C@@H]2O1)C=C)C Chemical compound CC1(O[C@@H]2C(=C[C@@H](N3C4=NC=NC(=C4C(=C3)F)Cl)[C@@H]2O1)C=C)C QYMUYMVEYDKDDH-RTXFEEFZSA-N 0.000 description 1
XMJFYRYHENGCTE-OIISXLGYSA-N CC1(O[C@@H]2C(=C[C@@H](N3C4=NC=NC(=C4C=C3)C(C)C)[C@@H]2O1)C=C)C Chemical compound CC1(O[C@@H]2C(=C[C@@H](N3C4=NC=NC(=C4C=C3)C(C)C)[C@@H]2O1)C=C)C XMJFYRYHENGCTE-OIISXLGYSA-N 0.000 description 1
HIBFLOGXFIARBM-OAGGEKHMSA-N CC1(O[C@@H]2[C@H](O1)C(=C[C@H]2N1C=CC2=C1N=CN=C2CC)C=C)C Chemical compound CC1(O[C@@H]2[C@H](O1)C(=C[C@H]2N1C=CC2=C1N=CN=C2CC)C=C)C HIBFLOGXFIARBM-OAGGEKHMSA-N 0.000 description 1
IMQUWOAJLOCLQP-ZACQAIPSSA-N CC1=C2C=CN([C@@H]3C=C(C=C)[C@H]4OC(C)(C)O[C@@H]34)C2=CC=N1 Chemical compound CC1=C2C=CN([C@@H]3C=C(C=C)[C@H]4OC(C)(C)O[C@@H]34)C2=CC=N1 IMQUWOAJLOCLQP-ZACQAIPSSA-N 0.000 description 1
VUNATOQGZYFTDJ-IIYDPXPESA-N CC[C@]12OC(C)(C)O[C@H]1[C@@H](C=C2C=O)n1ccc2c(Cl)ncnc12 Chemical compound CC[C@]12OC(C)(C)O[C@H]1[C@@H](C=C2C=O)n1ccc2c(Cl)ncnc12 VUNATOQGZYFTDJ-IIYDPXPESA-N 0.000 description 1
GYQCFNXGWVMZMB-LSQJDJJLSA-N CNC1=NC2=CC(OC(C)C3=C[C@H]([C@H](O)[C@@H]3O)N3C=CC4=C3N=CN=C4N)=CC=C2C=C1 Chemical compound CNC1=NC2=CC(OC(C)C3=C[C@H]([C@H](O)[C@@H]3O)N3C=CC4=C3N=CN=C4N)=CC=C2C=C1 GYQCFNXGWVMZMB-LSQJDJJLSA-N 0.000 description 1
XQRGLWMHXWYMRZ-UHFFFAOYSA-N COC1=CC=C(CC=2C(=NC3=CC=CC=C3C=2)N)C=C1 Chemical compound COC1=CC=C(CC=2C(=NC3=CC=CC=C3C=2)N)C=C1 XQRGLWMHXWYMRZ-UHFFFAOYSA-N 0.000 description 1
IASPXNPMKJMVRK-UHFFFAOYSA-N COC1=CC=C(CN(C2=NC3=CC(=CC=C3C=C2Cl)S)CC2=CC=C(C=C2)OC)C=C1 Chemical compound COC1=CC=C(CN(C2=NC3=CC(=CC=C3C=C2Cl)S)CC2=CC=C(C=C2)OC)C=C1 IASPXNPMKJMVRK-UHFFFAOYSA-N 0.000 description 1
JAEPPKKZRAIJAD-NLDZOOGBSA-N COC1=CC=C(CNC2=NC3=CC(CCC4=C[C@H]([C@@H]5OC(C)(C)O[C@H]45)N4C=CC5=C4N=CN=C5N)=CC=C3C=C2Br)C=C1 Chemical compound COC1=CC=C(CNC2=NC3=CC(CCC4=C[C@H]([C@@H]5OC(C)(C)O[C@H]45)N4C=CC5=C4N=CN=C5N)=CC=C3C=C2Br)C=C1 JAEPPKKZRAIJAD-NLDZOOGBSA-N 0.000 description 1
FAEPOYNSLWWICG-UHFFFAOYSA-N COc1cc2ccc(Br)cc2nc1N Chemical compound COc1cc2ccc(Br)cc2nc1N FAEPOYNSLWWICG-UHFFFAOYSA-N 0.000 description 1
BRDRJNWHDRFBRZ-UHFFFAOYSA-N CSC1=NC2=C(C=CC(Br)=C2)C11CCC1 Chemical compound CSC1=NC2=C(C=CC(Br)=C2)C11CCC1 BRDRJNWHDRFBRZ-UHFFFAOYSA-N 0.000 description 1
101100045312 Caenorhabditis elegans taf-4 gene Proteins 0.000 description 1
241000282472 Canis lupus familiaris Species 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
SZFKJCRPLGMEGM-SUFBMKPHSA-N ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@@]2([C@H]1OC(O2)(C)C)C)C(C)(C)O Chemical compound ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@@]2([C@H]1OC(O2)(C)C)C)C(C)(C)O SZFKJCRPLGMEGM-SUFBMKPHSA-N 0.000 description 1
WTVJLZKUMPIWTL-MZYLBHOOSA-N ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)CCC1=CC=C2C=CC(=NC2=C1)NC Chemical compound ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)CCC1=CC=C2C=CC(=NC2=C1)NC WTVJLZKUMPIWTL-MZYLBHOOSA-N 0.000 description 1
GSFKZAKVQWSDKS-QWQRMKEZSA-N ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@]2(OC(O[C@H]21)(C)C)CC)C=C Chemical compound ClC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@]2(OC(O[C@H]21)(C)C)CC)C=C GSFKZAKVQWSDKS-QWQRMKEZSA-N 0.000 description 1
NPIOJJBPDDADHZ-UHFFFAOYSA-N ClC=1C=[N+](C2=CC(=CC(=C2C=1)Cl)I)[O-] Chemical compound ClC=1C=[N+](C2=CC(=CC(=C2C=1)Cl)I)[O-] NPIOJJBPDDADHZ-UHFFFAOYSA-N 0.000 description 1
XJNKAZLXPROTTO-UPJWGTAASA-N ClC=1N=CC2=C(N=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)C=C Chemical compound ClC=1N=CC2=C(N=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)C=C XJNKAZLXPROTTO-UPJWGTAASA-N 0.000 description 1
CLIRNMDVVOGKAK-UHFFFAOYSA-N Clc1cc2c(Cl)cc(I)cc2nc1Cl Chemical compound Clc1cc2c(Cl)cc(I)cc2nc1Cl CLIRNMDVVOGKAK-UHFFFAOYSA-N 0.000 description 1
AAAWCMVYWMFIMR-UHFFFAOYSA-N Clc1cnc2cc(I)cc(Cl)c2c1 Chemical compound Clc1cnc2cc(I)cc(Cl)c2c1 AAAWCMVYWMFIMR-UHFFFAOYSA-N 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
102000006311 Cyclin D1 Human genes 0.000 description 1
108010058546 Cyclin D1 Proteins 0.000 description 1
102000013698 Cyclin-Dependent Kinase 6 Human genes 0.000 description 1
108010025468 Cyclin-Dependent Kinase 6 Proteins 0.000 description 1
229920000858 Cyclodextrin Polymers 0.000 description 1
HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
102100033996 Double-strand break repair protein MRE11 Human genes 0.000 description 1
239000006144 Dulbecco’s modiﬁed Eagle's medium Substances 0.000 description 1
240000006890 Erythroxylum coca Species 0.000 description 1
SCLMBBSRYRLVEH-UHFFFAOYSA-N FC1=NC2=CC(I)=CC=C2C=C1 Chemical compound FC1=NC2=CC(I)=CC=C2C=C1 SCLMBBSRYRLVEH-UHFFFAOYSA-N 0.000 description 1
QEGKBJLWRWIZIU-UHFFFAOYSA-N Fc1cc(Br)cc2nc(Cl)c(Br)cc12 Chemical compound Fc1cc(Br)cc2nc(Cl)c(Br)cc12 QEGKBJLWRWIZIU-UHFFFAOYSA-N 0.000 description 1
AWPCCITXXMJLSO-UHFFFAOYSA-N Fc1cc(Br)cc2ncc(Br)cc12 Chemical compound Fc1cc(Br)cc2ncc(Br)cc12 AWPCCITXXMJLSO-UHFFFAOYSA-N 0.000 description 1
IZAQGUATTVFGIL-UHFFFAOYSA-N Fc1cc2cc(Cl)c(Cl)nc2cc1Br Chemical compound Fc1cc2cc(Cl)c(Cl)nc2cc1Br IZAQGUATTVFGIL-UHFFFAOYSA-N 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
101710182396 Fibroblast growth factor receptor 3 Proteins 0.000 description 1
102100027842 Fibroblast growth factor receptor 3 Human genes 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
208000033962 Fontaine progeroid syndrome Diseases 0.000 description 1
102000020897 Formins Human genes 0.000 description 1
108091022623 Formins Proteins 0.000 description 1
238000003747 Grignard reaction Methods 0.000 description 1
208000002250 Hematologic Neoplasms Diseases 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
102000006947 Histones Human genes 0.000 description 1
101000591400 Homo sapiens Double-strand break repair protein MRE11 Proteins 0.000 description 1
LELOWRISYMNNSU-UHFFFAOYSA-N Hydrocyanic acid Natural products N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 1
101000618467 Hypocrea jecorina (strain ATCC 56765 / BCRC 32924 / NRRL 11460 / Rut C-30) Endo-1,4-beta-xylanase 2 Proteins 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
201000010743 Lambert-Eaton myasthenic syndrome Diseases 0.000 description 1
235000010643 Leucaena leucocephala Nutrition 0.000 description 1
240000007472 Leucaena leucocephala Species 0.000 description 1
206010058467 Lung neoplasm malignant Diseases 0.000 description 1
KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
239000004472 Lysine Substances 0.000 description 1
241000407429 Maja Species 0.000 description 1
241000600169 Maro Species 0.000 description 1
239000012359 Methanesulfonyl chloride Substances 0.000 description 1
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
108010050345 Microphthalmia-Associated Transcription Factor Proteins 0.000 description 1
102000013760 Microphthalmia-Associated Transcription Factor Human genes 0.000 description 1
LVDRREOUMKACNJ-BKMJKUGQSA-N N-[(2R,3S)-2-(4-chlorophenyl)-1-(1,4-dimethyl-2-oxoquinolin-7-yl)-6-oxopiperidin-3-yl]-2-methylpropane-1-sulfonamide Chemical compound CC(C)CS(=O)(=O)N[C@H]1CCC(=O)N([C@@H]1c1ccc(Cl)cc1)c1ccc2c(C)cc(=O)n(C)c2c1 LVDRREOUMKACNJ-BKMJKUGQSA-N 0.000 description 1
WCZKTUCDHDAAGU-UHFFFAOYSA-L N1=CC=CC=C1.[Cr](=O)(=O)(Cl)Cl Chemical compound N1=CC=CC=C1.[Cr](=O)(=O)(Cl)Cl WCZKTUCDHDAAGU-UHFFFAOYSA-L 0.000 description 1
MWOOQLIOESSPDJ-UHFFFAOYSA-N NC1=C(C=O)C(=CC(=C1)I)Cl Chemical compound NC1=C(C=O)C(=CC(=C1)I)Cl MWOOQLIOESSPDJ-UHFFFAOYSA-N 0.000 description 1
OVYYDRIJADZPHK-UHFFFAOYSA-N NC1=NC2=C(C=CC(Br)=C2)C11CCC1 Chemical compound NC1=NC2=C(C=CC(Br)=C2)C11CCC1 OVYYDRIJADZPHK-UHFFFAOYSA-N 0.000 description 1
YSPFXEOLLBCBCU-QRVBRYPASA-N NC1=NC2=C(C=CN2[C@@H]2C=C(CCC3=CC=C4C=C(Cl)C(N)=NC4=C3)[C@@H](O)[C@H]2O)C=N1 Chemical compound NC1=NC2=C(C=CN2[C@@H]2C=C(CCC3=CC=C4C=C(Cl)C(N)=NC4=C3)[C@@H](O)[C@H]2O)C=N1 YSPFXEOLLBCBCU-QRVBRYPASA-N 0.000 description 1
ACDACMNWOZAMFJ-UHFFFAOYSA-N NC1=NC2=CC(=CC=C2C=C1C#N)Br Chemical compound NC1=NC2=CC(=CC=C2C=C1C#N)Br ACDACMNWOZAMFJ-UHFFFAOYSA-N 0.000 description 1
AYQYNVYBDGEYKP-UHFFFAOYSA-N NC1=NC2=CC=CC=C2C=C1CC1CC1 Chemical compound NC1=NC2=CC=CC=C2C=C1CC1CC1 AYQYNVYBDGEYKP-UHFFFAOYSA-N 0.000 description 1
SUJNFJXBEXCVOM-QRVBRYPASA-N NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC=C3C=C(F)C(N)=NC3=C2)[C@@H](O)[C@H]1O Chemical compound NC1=NC=NC2=C1C=CN2[C@@H]1C=C(CCC2=CC=C3C=C(F)C(N)=NC3=C2)[C@@H](O)[C@H]1O SUJNFJXBEXCVOM-QRVBRYPASA-N 0.000 description 1
GDWJXHFFIYGWDC-NRSPTQNISA-N NC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]([C@H]1O)O)CCC1=CC=C2C=CC(=NC2=C1)NC Chemical compound NC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]([C@H]1O)O)CCC1=CC=C2C=CC(=NC2=C1)NC GDWJXHFFIYGWDC-NRSPTQNISA-N 0.000 description 1
POZYLHOLLDMCCT-MZYLBHOOSA-N NC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)CCC1=CC=C2C=CC(=NC2=C1)NC Chemical compound NC=1C2=C(N=CN=1)N(C=C2)[C@@H]1C=C([C@H]2OC(O[C@H]21)(C)C)CCC1=CC=C2C=CC(=NC2=C1)NC POZYLHOLLDMCCT-MZYLBHOOSA-N 0.000 description 1
GCTSQEFPZJMFGI-UHFFFAOYSA-N Nc1nc2cc(Br)c(F)cc2cc1Cl Chemical compound Nc1nc2cc(Br)c(F)cc2cc1Cl GCTSQEFPZJMFGI-UHFFFAOYSA-N 0.000 description 1
LEEQXLVAKAUGLZ-UHFFFAOYSA-N Nc1nc2cc(I)cc(Cl)c2cc1Cl Chemical compound Nc1nc2cc(I)cc(Cl)c2cc1Cl LEEQXLVAKAUGLZ-UHFFFAOYSA-N 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
CQGDSNPYXSLEDA-UHFFFAOYSA-N O1C(OC2C1=CC=C2)N Chemical compound O1C(OC2C1=CC=C2)N CQGDSNPYXSLEDA-UHFFFAOYSA-N 0.000 description 1
229910019213 POCl3 Inorganic materials 0.000 description 1
229940125897 PRMT5 inhibitor Drugs 0.000 description 1
101150003085 Pdcl gene Proteins 0.000 description 1
235000019483 Peanut oil Nutrition 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
101710097214 Protein N-terminal asparagine amidohydrolase Proteins 0.000 description 1
102100034233 Protein N-terminal asparagine amidohydrolase Human genes 0.000 description 1
101710084434 Protein arginine N-methyltransferase 1 Proteins 0.000 description 1
102000004389 Ribonucleoproteins Human genes 0.000 description 1
108010081734 Ribonucleoproteins Proteins 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
101000921780 Solanum tuberosum Cysteine synthase Proteins 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
229910052776 Thorium Inorganic materials 0.000 description 1
241000927721 Tritia Species 0.000 description 1
108700025716 Tumor Suppressor Genes Proteins 0.000 description 1
102000044209 Tumor Suppressor Genes Human genes 0.000 description 1
FTSCTBXDNZMKIR-NLDZOOGBSA-N [(3aR,6R,6aS)-2,2-dimethyl-6-(4-methylpyrrolo[2,3-d]pyrimidin-7-yl)-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methoxy-tert-butyl-diphenylsilane Chemical compound CC1=NC=NC2=C1C=CN2[C@@H]1C=C(CO[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)[C@H]2OC(C)(C)O[C@@H]12 FTSCTBXDNZMKIR-NLDZOOGBSA-N 0.000 description 1
VCGRCGATWJFBKK-PFBJBMPXSA-N [(3aR,6R,6aS)-6-(2-chloropyrrolo[2,3-d]pyrimidin-7-yl)-2,2-dimethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methoxy-tert-butyl-diphenylsilane Chemical compound CC(C)(C)[Si](OCC1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=C(Cl)N=C2)(C1=CC=CC=C1)C1=CC=CC=C1 VCGRCGATWJFBKK-PFBJBMPXSA-N 0.000 description 1
LLCPGHUMQAFFBB-IEUSDUHPSA-N [(3aR,6R,6aS)-6-(4-chloro-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl)-2,2-dimethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methoxy-tert-butyl-diphenylsilane Chemical compound CC(C)(C)[Si](OCC1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=C(F)C2=C1N=CN=C2Cl)(C1=CC=CC=C1)C1=CC=CC=C1 LLCPGHUMQAFFBB-IEUSDUHPSA-N 0.000 description 1
RWBAAVWGXYVZBO-PFBJBMPXSA-N [(3aR,6R,6aS)-6-(4-chloropyrrolo[2,3-d]pyrimidin-7-yl)-2,2-dimethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]methoxy-tert-butyl-diphenylsilane Chemical compound CC(C)(C)[Si](OCC1=C[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=CC2=C1N=CN=C2Cl)(C1=CC=CC=C1)C1=CC=CC=C1 RWBAAVWGXYVZBO-PFBJBMPXSA-N 0.000 description 1
KOOADCGQJDGAGA-UHFFFAOYSA-N [amino(dimethyl)silyl]methane Chemical compound C[Si](C)(C)N KOOADCGQJDGAGA-UHFFFAOYSA-N 0.000 description 1
125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000008272 agar Substances 0.000 description 1
235000010419 agar Nutrition 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000000539 amino acid group Chemical group 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
239000003708 ampul Substances 0.000 description 1
125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
101150117004 atg18 gene Proteins 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000012752 auxiliary agent Substances 0.000 description 1
125000002393 azetidinyl group Chemical group 0.000 description 1
210000003719 b-lymphocyte Anatomy 0.000 description 1
210000002469 basement membrane Anatomy 0.000 description 1
150000007514 bases Chemical class 0.000 description 1
OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
SIKJAQJRHWYJAI-UHFFFAOYSA-N benzopyrrole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
125000002619 bicyclic group Chemical group 0.000 description 1
MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
102000023732 binding proteins Human genes 0.000 description 1
108091008324 binding proteins Proteins 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000008280 blood Substances 0.000 description 1
ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 1
235000008429 bread Nutrition 0.000 description 1
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
238000004113 cell culture Methods 0.000 description 1
230000022131 cell cycle Effects 0.000 description 1
230000030833 cell death Effects 0.000 description 1
230000003915 cell function Effects 0.000 description 1
239000013592 cell lysate Substances 0.000 description 1
238000012054 celltiter-glo Methods 0.000 description 1
230000033077 cellular process Effects 0.000 description 1
230000005754 cellular signaling Effects 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
235000010980 cellulose Nutrition 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
VYLVYHXQOHJDJL-UHFFFAOYSA-K cerium trichloride Chemical compound Cl[Ce](Cl)Cl VYLVYHXQOHJDJL-UHFFFAOYSA-K 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
229940068682 chewable tablet Drugs 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 description 1
235000008957 cocaer Nutrition 0.000 description 1
ZPUCINDJVBIVPJ-LJISPDSOSA-N ***e Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 1
KZZKOVLJUKWSKX-UHFFFAOYSA-N cyclobutanamine Chemical compound NC1CCC1 KZZKOVLJUKWSKX-UHFFFAOYSA-N 0.000 description 1
125000006311 cyclobutyl amino group Chemical group [H]N(*)C1([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
JMYVMOUINOAAPA-UHFFFAOYSA-N cyclopropanecarbaldehyde Chemical compound O=CC1CC1 JMYVMOUINOAAPA-UHFFFAOYSA-N 0.000 description 1
GUDMZGLFZNLYEY-UHFFFAOYSA-N cyclopropylmethanol Chemical compound OCC1CC1 GUDMZGLFZNLYEY-UHFFFAOYSA-N 0.000 description 1
210000000805 cytoplasm Anatomy 0.000 description 1
125000005507 decahydroisoquinolyl group Chemical group 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
230000008021 deposition Effects 0.000 description 1
238000000151 deposition Methods 0.000 description 1
230000002074 deregulated effect Effects 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
125000004774 dichlorofluoromethyl group Chemical group FC(Cl)(Cl)* 0.000 description 1
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
125000004982 dihaloalkyl group Chemical group 0.000 description 1
208000037765 diseases and disorders Diseases 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000002255 enzymatic effect Effects 0.000 description 1
210000002615 epidermis Anatomy 0.000 description 1
LJQKCYFTNDAAPC-UHFFFAOYSA-N ethanol;ethyl acetate Chemical compound CCO.CCOC(C)=O LJQKCYFTNDAAPC-UHFFFAOYSA-N 0.000 description 1
125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
230000005284 excitation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
235000003599 food sweetener Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000012458 free base Substances 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
238000003304 gavage Methods 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
239000010931 gold Substances 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
125000000487 histidyl group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C([H])=N1 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
230000006607 hypermethylation Effects 0.000 description 1
125000002883 imidazolyl group Chemical group 0.000 description 1
238000001727 in vivo Methods 0.000 description 1
125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 description 1
125000001041 indolyl group Chemical group 0.000 description 1
230000036512 infertility Effects 0.000 description 1
230000003993 interaction Effects 0.000 description 1
238000007918 intramuscular administration Methods 0.000 description 1
238000007915 intraurethral administration Methods 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
125000003384 isochromanyl group Chemical group C1(OCCC2=CC=CC=C12)* 0.000 description 1
125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 description 1
125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 1
125000005956 isoquinolyl group Chemical group 0.000 description 1
125000004628 isothiazolidinyl group Chemical group S1N(CCC1)* 0.000 description 1
125000001786 isothiazolyl group Chemical group 0.000 description 1
125000003965 isoxazolidinyl group Chemical group 0.000 description 1
125000000842 isoxazolyl group Chemical group 0.000 description 1
239000008101 lactose Substances 0.000 description 1
CFHGBZLNZZVTAY-UHFFFAOYSA-N lawesson's reagent Chemical compound C1=CC(OC)=CC=C1P1(=S)SP(=S)(C=2C=CC(OC)=CC=2)S1 CFHGBZLNZZVTAY-UHFFFAOYSA-N 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
239000011344 liquid material Substances 0.000 description 1
239000006193 liquid solution Substances 0.000 description 1
239000006194 liquid suspension Substances 0.000 description 1
239000007937 lozenge Substances 0.000 description 1
201000005202 lung cancer Diseases 0.000 description 1
208000020816 lung neoplasm Diseases 0.000 description 1
208000025036 lymphosarcoma Diseases 0.000 description 1
239000006166 lysate Substances 0.000 description 1
239000012139 lysis buffer Substances 0.000 description 1
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
239000001095 magnesium carbonate Substances 0.000 description 1
229910000021 magnesium carbonate Inorganic materials 0.000 description 1
235000019359 magnesium stearate Nutrition 0.000 description 1
VFZXMEQGIIWBFJ-UHFFFAOYSA-M magnesium;cyclopropane;bromide Chemical compound [Mg+2].[Br-].C1C[CH-]1 VFZXMEQGIIWBFJ-UHFFFAOYSA-M 0.000 description 1
YCCXQARVHOPWFJ-UHFFFAOYSA-M magnesium;ethane;chloride Chemical compound [Mg+2].[Cl-].[CH2-]C YCCXQARVHOPWFJ-UHFFFAOYSA-M 0.000 description 1
LVKCSZQWLOVUGB-UHFFFAOYSA-M magnesium;propane;bromide Chemical compound [Mg+2].[Br-].C[CH-]C LVKCSZQWLOVUGB-UHFFFAOYSA-M 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
230000036210 malignancy Effects 0.000 description 1
CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
230000035800 maturation Effects 0.000 description 1
QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
OKKJLVBELUTLKV-VMNATFBRSA-N methanol-d1 Chemical compound [2H]OC OKKJLVBELUTLKV-VMNATFBRSA-N 0.000 description 1
239000003697 methyltransferase inhibitor Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
125000002757 morpholinyl group Chemical group 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
QPHYISQSHYVPRT-UHFFFAOYSA-N n-[(4-methoxyphenyl)methyl]quinolin-2-amine Chemical compound C1=CC(OC)=CC=C1CNC1=CC=C(C=CC=C2)C2=N1 QPHYISQSHYVPRT-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
POVSMFKXVSNGSU-UHFFFAOYSA-N n-methylquinolin-2-amine Chemical compound C1=CC=CC2=NC(NC)=CC=C21 POVSMFKXVSNGSU-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
125000005060 octahydroindolyl group Chemical group N1(CCC2CCCCC12)* 0.000 description 1
125000005061 octahydroisoindolyl group Chemical group C1(NCC2CCCCC12)* 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
235000008390 olive oil Nutrition 0.000 description 1
239000002997 ophthalmic solution Substances 0.000 description 1
229940054534 ophthalmic solution Drugs 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
125000000160 oxazolidinyl group Chemical group 0.000 description 1
125000005968 oxazolinyl group Chemical group 0.000 description 1
125000002971 oxazolyl group Chemical group 0.000 description 1
LVSJDHGRKAEGLX-UHFFFAOYSA-N oxolane;2,2,2-trifluoroacetic acid Chemical compound C1CCOC1.OC(=O)C(F)(F)F LVSJDHGRKAEGLX-UHFFFAOYSA-N 0.000 description 1
NXJCBFBQEVOTOW-UHFFFAOYSA-L palladium(2+);dihydroxide Chemical compound O[Pd]O NXJCBFBQEVOTOW-UHFFFAOYSA-L 0.000 description 1
YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000000312 peanut oil Substances 0.000 description 1
239000001814 pectin Substances 0.000 description 1
235000010987 pectin Nutrition 0.000 description 1
229920001277 pectin Polymers 0.000 description 1
239000008188 pellet Substances 0.000 description 1
239000008177 pharmaceutical agent Substances 0.000 description 1
239000000825 pharmaceutical preparation Substances 0.000 description 1
125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
229940023488 pill Drugs 0.000 description 1
125000004193 piperazinyl group Chemical group 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
238000001637 plasma atomic emission spectroscopy Methods 0.000 description 1
229920000110 poly(aryl ether sulfone) Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
230000029279 positive regulation of transcription, DNA-dependent Effects 0.000 description 1
230000004481 post-translational protein modification Effects 0.000 description 1
235000011056 potassium acetate Nutrition 0.000 description 1
JLKDVMWYMMLWTI-UHFFFAOYSA-M potassium iodate Chemical compound [K+].[O-]I(=O)=O JLKDVMWYMMLWTI-UHFFFAOYSA-M 0.000 description 1
239000001230 potassium iodate Substances 0.000 description 1
235000006666 potassium iodate Nutrition 0.000 description 1
229940093930 potassium iodate Drugs 0.000 description 1
229910000160 potassium phosphate Inorganic materials 0.000 description 1
235000011009 potassium phosphates Nutrition 0.000 description 1
LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical group [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
239000012256 powdered iron Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
210000002307 prostate Anatomy 0.000 description 1
230000004952 protein activity Effects 0.000 description 1
230000019639 protein methylation Effects 0.000 description 1
125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
230000002685 pulmonary effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
125000003373 pyrazinyl group Chemical group 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
CLKZWXHKFXZIMA-UHFFFAOYSA-N pyrinuron Chemical group C1=CC([N+](=O)[O-])=CC=C1NC(=O)NCC1=CC=CN=C1 CLKZWXHKFXZIMA-UHFFFAOYSA-N 0.000 description 1
125000000719 pyrrolidinyl group Chemical group 0.000 description 1
125000000168 pyrrolyl group Chemical group 0.000 description 1
JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
WDXARTMCIRVMAE-UHFFFAOYSA-N quinoline-2-carbonitrile Chemical compound C1=CC=CC2=NC(C#N)=CC=C21 WDXARTMCIRVMAE-UHFFFAOYSA-N 0.000 description 1
125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
125000004621 quinuclidinyl group Chemical group N12C(CC(CC1)CC2)* 0.000 description 1
238000006268 reductive amination reaction Methods 0.000 description 1
230000008439 repair process Effects 0.000 description 1
230000004043 responsiveness Effects 0.000 description 1
238000012552 review Methods 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
239000012056 semi-solid material Substances 0.000 description 1
230000019491 signal transduction Effects 0.000 description 1
150000003384 small molecules Chemical class 0.000 description 1
ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 1
KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
239000011343 solid material Substances 0.000 description 1
MXXGFDQBAJVZQC-UHFFFAOYSA-N spiro[cyclobutane-1,3'-indole] Chemical compound C1CC2(C1)C=NC1=C2C=CC=C1 MXXGFDQBAJVZQC-UHFFFAOYSA-N 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
239000012089 stop solution Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
238000004808 supercritical fluid chromatography Methods 0.000 description 1
230000004083 survival effect Effects 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
239000003765 sweetening agent Substances 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000010998 test method Methods 0.000 description 1
WNDHBMUTTTWRJA-UHFFFAOYSA-N tetrahydridosulfur Chemical compound [SH4] WNDHBMUTTTWRJA-UHFFFAOYSA-N 0.000 description 1
125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
125000003831 tetrazolyl group Chemical group 0.000 description 1
238000011287 therapeutic dose Methods 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
125000001113 thiadiazolyl group Chemical group 0.000 description 1
125000006089 thiamorpholinyl sulfoxide group Chemical group 0.000 description 1
125000001984 thiazolidinyl group Chemical group 0.000 description 1
125000002769 thiazolinyl group Chemical group 0.000 description 1
125000000335 thiazolyl group Chemical group 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
229940100615 topical ointment Drugs 0.000 description 1
125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
238000007070 tosylation reaction Methods 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
238000012546 transfer Methods 0.000 description 1
125000004306 triazinyl group Chemical group 0.000 description 1
125000001425 triazolyl group Chemical group 0.000 description 1
KPZSTOVTJYRDIO-UHFFFAOYSA-K trichlorocerium;heptahydrate Chemical compound O.O.O.O.O.O.O.Cl[Ce](Cl)Cl KPZSTOVTJYRDIO-UHFFFAOYSA-K 0.000 description 1
CMSYDJVRTHCWFP-UHFFFAOYSA-N triphenylphosphane;hydrobromide Chemical compound Br.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 CMSYDJVRTHCWFP-UHFFFAOYSA-N 0.000 description 1
230000003827 upregulation Effects 0.000 description 1
238000012795 verification Methods 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
General Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Public Health (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Epidemiology (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

BR112020011746-3A 2017-12-13 2018-12-13 compostos heterocíclicos bicíclicos substituídos atuando como inibidores de prmt5 BR112020011746A2 (pt)

Applications Claiming Priority (7)

Application Number	Priority Date	Filing Date	Title
IN201721044886		2017-12-13
IN201721044886		2017-12-13
IN201821024634		2018-07-02
IN201821024634		2018-07-02
IN201821040029		2018-10-23
IN201821040029		2018-10-23
PCT/IB2018/060015 WO2019116302A1 (en)	2017-12-13	2018-12-13	Substituted bicyclic heterocyclic compounds as prmt5 inhibitors

Publications (1)

Publication Number	Publication Date
BR112020011746A2 true BR112020011746A2 (pt)	2020-11-17

Family

ID=65036860

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BR112020011746-3A BR112020011746A2 (pt)	2017-12-13	2018-12-13	compostos heterocíclicos bicíclicos substituídos atuando como inibidores de prmt5

Country Status (28)

Country	Link
US (2)	US11459330B2 (ja)
EP (1)	EP3724190B1 (ja)
JP (1)	JP7282778B2 (ja)
KR (1)	KR20200098598A (ja)
CN (1)	CN111712498B (ja)
AU (1)	AU2018385664B2 (ja)
BR (1)	BR112020011746A2 (ja)
CA (1)	CA3085259A1 (ja)
CL (1)	CL2020001576A1 (ja)
CR (1)	CR20200263A (ja)
CU (1)	CU24621B1 (ja)
DK (1)	DK3724190T3 (ja)
ES (1)	ES2927860T3 (ja)
GE (1)	GEP20227359B (ja)
HR (1)	HRP20221207T1 (ja)
HU (1)	HUE059945T2 (ja)
IL (1)	IL274936B2 (ja)
LT (1)	LT3724190T (ja)
MX (1)	MX2020006181A (ja)
PE (1)	PE20211444A1 (ja)
PH (1)	PH12020550881A1 (ja)
PL (1)	PL3724190T3 (ja)
PT (1)	PT3724190T (ja)
RS (1)	RS63623B1 (ja)
SG (1)	SG11202004934QA (ja)
UA (1)	UA126349C2 (ja)
WO (1)	WO2019116302A1 (ja)
ZA (1)	ZA202003528B (ja)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US11077101B1 (en)	2018-07-18	2021-08-03	Tango Therapeutics, Inc.	Compounds and methods of use
WO2020081257A1 (en)	2018-10-05	2020-04-23	Vertex Pharmaceuticals Incorporated	Modulators of alpha-1 antitrypsin
AU2020256166A1 (en) *	2019-04-02	2021-10-14	Aligos Therapeutics, Inc.	Compounds targeting PRMT5
UY38696A (es)	2019-05-14	2020-11-30	Vertex Pharma	Moduladores de alfa-1 antitripsina
CN114126614A (zh) *	2019-05-30	2022-03-01	安杰斯制药公司	作为prmt5抑制剂的杂环化合物
JP2022536337A (ja) *	2019-06-10	2022-08-15	ルピン・リミテッド	Ｐｒｍｔ５阻害剤
KR20220086628A (ko)	2019-10-22	2022-06-23	루핀 리미티드	Prmt5 저해제의 약학적 조합물
US20220372040A1 (en) *	2019-10-25	2022-11-24	Accent Therapeutics, Inc.	Mettl3 modulators
WO2021111322A1 (en)	2019-12-03	2021-06-10	Lupin Limited	Substituted nucleoside analogs as prmt5 inhibitors
US20220112194A1 (en) *	2020-04-01	2022-04-14	Aligos Therapeutics, Inc.	Compounds targeting prmt5
CA3179189A1 (en) *	2020-04-03	2021-10-07	Vertex Pharmaceuticals Incorporated	Modulators of alpha-1 antitrypsin
JP2023536589A (ja)	2020-07-31	2023-08-28	タンゴセラピューティクス，インコーポレイテッド	Ｍｔａｐ欠損及び／またはｍｔａ蓄積癌の治療に有用なピペリジン－１－イル－ｎ－ピリジン－３－イル－２－オキソアセトアミド誘導体
CA3203205A1 (en)	2021-01-19	2022-07-28	Mandar Ramesh Bhonde	Pharmaceutical combinations of sos1 inhibitors for treating and/or preventing cancer
CN113234079B (zh) *	2021-04-30	2022-02-01	上海湃隆生物科技有限公司	用作prmt5抑制剂的核苷类似物

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU2003251431A1 (en)	2002-07-22	2004-02-09	Cambridge University Technical Services Ltd.	Synthesis of discodermolide
WO2005016878A2 (en)	2003-08-13	2005-02-24	Isis Pharmaceuticals, Inc.	METHODS FOR THE PREPARATION OF 5-FLUORO-PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
WO2006091905A1 (en)	2005-02-25	2006-08-31	Gilead Sciences, Inc.	Bicyclo (3.1.0) hexane derivatives as antiviral compounds
EP2049490A1 (en)	2006-06-09	2009-04-22	Astra Zeneca AB	N-(benzoyl)-o- [2- (pyridin- 2 -ylamino) ethyl]-l-tyrosine derivatives and related compounds as a5b1 antagonists for the treatment of solid tumors
ES2381446T3 (es)	2007-03-08	2012-05-28	Janssen Pharmaceutica, N.V.	Derivado de quinolinona como inhibidores de PARP y TANK
FR2926556B1 (fr)	2008-01-22	2010-02-19	Sanofi Aventis	Derives de carboxamides n-azabicycliques, leur preparation et leur application en therapeutique
WO2010036213A1 (en)	2008-09-26	2010-04-01	Agency For Science, Technology And Research	3-deazaneplanocin derivatives
US9044432B2 (en)	2009-12-22	2015-06-02	Ohio State Innovation Foundation	Compositions and methods for cancer detection and treatment
GB0922332D0 (en)	2009-12-22	2010-02-03	Isis Innovation	Method of treatment and screening method
CA2803842C (en)	2010-06-30	2020-01-07	Fujifilm Corporation	Nicotinamide derivative or salt thereof as syk-inhibitors
WO2012037108A1 (en)	2010-09-13	2012-03-22	Glaxosmithkline Llc	Aminoquinoline derivatives as antiviral agents
WO2012123298A1 (en)	2011-03-11	2012-09-20	F. Hoffmann-La Roche Ag	Antiviral compounds
ES2608053T3 (es)	2011-08-19	2017-04-05	Glaxosmithkline Intellectual Property (No. 2) Limited	Inhibidores de ácido graso sintasa
WO2013157022A1 (en) *	2012-04-20	2013-10-24	Advinus Therapeutics Limited	Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof
BR112014030630A2 (pt)	2012-06-08	2017-06-27	Gilead Sciences Inc	inibidores macrocíclicos de vírus flaviviridae
WO2014008223A2 (en)	2012-07-03	2014-01-09	Glaxosmithkline Llc	Fatty acid synthase inhibitors
EP2935240A1 (en)	2012-12-21	2015-10-28	Epizyme, Inc.	Prmt5 inhibitors and uses thereof
EA027908B1 (ru)	2012-12-21	2017-09-29	Эпизим, Инк.	Ингибиторы prmt5 и их применения
CA2894157A1 (en)	2012-12-21	2014-06-26	Epizyme, Inc.	Prmt5 inhibitors and uses thereof
EP2935241A1 (en)	2012-12-21	2015-10-28	Epizyme, Inc.	Prmt5 inhibitors and uses thereof
WO2014100730A1 (en)	2012-12-21	2014-06-26	Epizyme, Inc.	Prmt5 inhibitors containing a dihydro- or tetrahydroisoquinoline and uses thereof
CA2897200C (en)	2013-01-14	2021-07-06	Incyte Corporation	Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors
GB201302927D0 (en)	2013-02-20	2013-04-03	Cancer Therapeutics Crc Pty Ltd	Compounds
CA2942833A1 (en)	2013-03-15	2014-09-18	Ohio State Innovation Foundation	Inhibitors of prmt5 and methods of their use
SG11201602662YA (en)	2013-10-10	2016-05-30	Araxes Pharma Llc	Inhibitors of kras g12c
RU2697512C2 (ru)	2014-05-22	2019-08-15	Ф. Хоффманн-Ля Рош Аг	Производные индолин-2-она и 1,3-дигидро-пирроло[3,2-c]пиридин-2-она
EP3160466A4 (en)	2014-06-25	2017-12-27	Epizyme, Inc.	Prmt5 inhibitors and uses thereof
KR102493854B1 (ko)	2014-06-25	2023-01-30	글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드	(s)-6-((1-아세틸피페리딘-4-일)아미노)-n-(3-(3,4-디히드로이소퀴놀린-2(1h)-일)-2-히드록시프로필)피리미딘-4-카르복스아미드의 결정질 염
US20170198006A1 (en)	2014-06-25	2017-07-13	Epizyme, Inc.	Prmt5 inhibitors and uses thereof
CA2953572A1 (en)	2014-08-04	2016-02-11	Epizyme, Inc.	Prmt5 inhibitors and uses thereof
US10005792B2 (en)	2014-09-03	2018-06-26	Ctxt Pty. Ltd.	Aminoindane-, aminotetrahydronaphthalene- and aminobenzocyclobutane-derived PRMT5-inhibitors
GB201415573D0 (en)	2014-09-03	2014-10-15	Cancer Therapeutics Crc Pty Ltd	Compounds
US10494376B2 (en)	2014-09-03	2019-12-03	Ctxt Pty. Ltd.	Tetrahydroisoquinoline derived PRMT5-inhibitors
WO2016038550A1 (en)	2014-09-11	2016-03-17	Novartis Ag	Inhibition of prmt5 to treat mtap-deficiency-related diseases
CR20170384A (es)	2015-02-24	2017-11-16	Pfizer	Derivados de nucleosidos sustituidos utiles como agentes antineoplasicos
WO2016145150A2 (en)	2015-03-11	2016-09-15	The Broad Institute Inc.	Selective treatment of prmt5 dependent cancer
AR104326A1 (es)	2015-05-04	2017-07-12	Lilly Co Eli	Compuestos nucleósidos 5-sustituidos
TW202321249A (zh)	2015-08-26	2023-06-01	比利時商健生藥品公司	使用作為ｐｒｍｔ５抑制劑之新穎經６－６雙環芳香環取代之核苷類似物
AU2016355433C1 (en)	2015-11-16	2021-12-16	Araxes Pharma Llc	2-substituted quinazoline compounds comprising a substituted heterocyclic group and methods of use thereof
EA201990851A1 (ru) *	2017-02-24	2019-09-30	Янссен Фармацевтика Нв	Новые аналоги карбануклеозида, замещенные моноциклической и бициклической кольцевой системой, для применения в качестве ингибиторов prmt5

2018
- 2018-12-13 ES ES18836520T patent/ES2927860T3/es active Active
- 2018-12-13 SG SG11202004934QA patent/SG11202004934QA/en unknown
- 2018-12-13 BR BR112020011746-3A patent/BR112020011746A2/pt unknown
- 2018-12-13 PT PT188365209T patent/PT3724190T/pt unknown
- 2018-12-13 CA CA3085259A patent/CA3085259A1/en active Pending
- 2018-12-13 HR HRP20221207TT patent/HRP20221207T1/hr unknown
- 2018-12-13 RS RS20220931A patent/RS63623B1/sr unknown
- 2018-12-13 PE PE2020000761A patent/PE20211444A1/es unknown
- 2018-12-13 MX MX2020006181A patent/MX2020006181A/es unknown
- 2018-12-13 PL PL18836520.9T patent/PL3724190T3/pl unknown
- 2018-12-13 CN CN201880089329.6A patent/CN111712498B/zh active Active
- 2018-12-13 JP JP2020532614A patent/JP7282778B2/ja active Active
- 2018-12-13 LT LTEPPCT/IB2018/060015T patent/LT3724190T/lt unknown
- 2018-12-13 DK DK18836520.9T patent/DK3724190T3/da active
- 2018-12-13 KR KR1020207019844A patent/KR20200098598A/ko not_active Application Discontinuation
- 2018-12-13 IL IL274936A patent/IL274936B2/en unknown
- 2018-12-13 EP EP18836520.9A patent/EP3724190B1/en active Active
- 2018-12-13 WO PCT/IB2018/060015 patent/WO2019116302A1/en unknown
- 2018-12-13 GE GEAP201815385A patent/GEP20227359B/en unknown
- 2018-12-13 UA UAA202004140A patent/UA126349C2/uk unknown
- 2018-12-13 AU AU2018385664A patent/AU2018385664B2/en active Active
- 2018-12-13 US US16/772,959 patent/US11459330B2/en active Active
- 2018-12-13 CU CU2020000051A patent/CU24621B1/es unknown
- 2018-12-13 HU HUE18836520A patent/HUE059945T2/hu unknown
- 2018-12-13 CR CR20200263A patent/CR20200263A/es unknown
2020
- 2020-06-06 PH PH12020550881A patent/PH12020550881A1/en unknown
- 2020-06-11 CL CL2020001576A patent/CL2020001576A1/es unknown
- 2020-06-12 ZA ZA2020/03528A patent/ZA202003528B/en unknown
2022
- 2022-05-06 US US17/738,370 patent/US11952380B2/en active Active

Also Published As

Publication number	Publication date
US20220267339A1 (en)	2022-08-25
US20210163486A1 (en)	2021-06-03
HUE059945T2 (hu)	2023-01-28
PH12020550881A1 (en)	2021-04-05
HRP20221207T1 (hr)	2022-12-09
KR20200098598A (ko)	2020-08-20
ES2927860T3 (es)	2022-11-11
CL2020001576A1 (es)	2020-11-06
WO2019116302A1 (en)	2019-06-20
CN111712498A (zh)	2020-09-25
CR20200263A (es)	2020-07-26
CN111712498B (zh)	2023-09-29
IL274936B1 (en)	2023-05-01
RS63623B1 (sr)	2022-10-31
CU24621B1 (es)	2022-09-08
EP3724190A1 (en)	2020-10-21
EP3724190B1 (en)	2022-07-06
US11459330B2 (en)	2022-10-04
GEP20227359B (en)	2022-03-10
PL3724190T3 (pl)	2022-10-31
MX2020006181A (es)	2020-09-03
JP2021506793A (ja)	2021-02-22
UA126349C2 (uk)	2022-09-21
PE20211444A1 (es)	2021-08-05
ZA202003528B (en)	2022-05-25
IL274936A (en)	2020-07-30
CU20200051A7 (es)	2021-03-11
CA3085259A1 (en)	2019-06-20
AU2018385664A1 (en)	2020-07-02
PT3724190T (pt)	2022-10-03
US11952380B2 (en)	2024-04-09
DK3724190T3 (da)	2022-10-10
JP7282778B2 (ja)	2023-05-29
LT3724190T (lt)	2022-10-10
AU2018385664B2 (en)	2022-06-02
SG11202004934QA (en)	2020-07-29
IL274936B2 (en)	2023-09-01

Legal Events

Date	Code	Title	Description
2021-12-07	B350	Update of information on the portal [chapter 15.35 patent gazette]
2022-09-20	B06W	Patent application suspended after preliminary examination (for patents with searches from other patent authorities) chapter 6.23 patent gazette]

Publication	Publication Date	Title
BR112020011746A2 (pt)	2020-11-17	compostos heterocíclicos bicíclicos substituídos atuando como inibidores de prmt5
TWI714567B (zh)	2021-01-01	作為lsd1抑制劑之雜環化合物
JP2022506887A (ja)	2022-01-17	窒素含有縮合複素環系ｓｈｐ２阻害剤化合物、製造方法及び使用
CA2897333C (en)	2021-07-06	Thiazolecarboxamides and pyridinecarboxamide compounds useful as pim kinase inhibitors
KR101716011B1 (ko)	2017-03-13	Btk 활성의 억제제인 알킬화된 피페라진 화합물
CN112739690A (zh)	2021-04-30	用作smarca2拮抗剂的吡啶-2-酮化合物
KR20180043794A (ko)	2018-04-30	피라졸 피리미딘 유도체 및 이의 용도
JP6888006B2 (ja)	2021-06-16	Ｍｎｋ１およびｍｎｋ２を阻害するピロロ−、ピラゾロ−、イミダゾ−ピリミジンおよびピリジン化合物
TW201307292A (zh)	2013-02-16	經取代之６，６－稠合含氮雜環化合物及其用途
KR20140096100A (ko)	2014-08-04	이환 피페라진 화합물
CN113135910A (zh)	2021-07-20	嘧啶-4(3h)-酮类杂环化合物、其制备方法及其在医药学上的应用
KR20110015699A (ko)	2011-02-16	디아자카르바졸 및 사용 방법
JP7357146B2 (ja)	2023-10-05	アザヘテロアリール化合物及びその使用
CA3114259A1 (en)	2020-04-02	Aminonorbornane derivative and manufacture method therefor and use thereof
CA3181909A1 (en)	2021-12-16	4-ethynylpyridine derivatives useful as gcn2 inhibitors
KR20200138306A (ko)	2020-12-09	헤테로시클릭 화합물
CN114380818A (zh)	2022-04-22	吡唑并吡啶类化合物，及其药物组合物、制备方法和用途
CN112694477B (zh)	2024-02-06	吡唑并环类化合物，包含其的药物组合物，其制备方法及其用途
CN116249692A (zh)	2023-06-09	吡唑类化合物及其制备方法和用途
EA041973B1 (ru)	2022-12-21	Замещенные бициклические гетероциклические соединения в качестве ингибиторов prmt5
WO2020247679A1 (en)	2020-12-10	Wdr5 inhibitors and modulators
CN116262750A (zh)	2023-06-16	一种芳杂环类化合物及其制备方法和用途
JP2024518784A (ja)	2024-05-02	含窒素複素環式化合物
OA19533A (en)	2020-11-13	Substituted bicyclic heterocyclic compounds as PRMT5 inhibitors.
KR20110015627A (ko)	2011-02-16	치환된 피롤 및 사용 방법